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Chemistry

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Also known as: 7647-14-5, Salt, Table salt, Halite, Saline, Rock salt
Molecular Formula
ClNa
Molecular Weight
58.44  g/mol
InChI Key
FAPWRFPIFSIZLT-UHFFFAOYSA-M
FDA UNII
451W47IQ8X

Sodium Chloride
A ubiquitous sodium salt that is commonly used to season food.
1 2D Structure

Sodium Chloride

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
sodium;chloride
2.1.2 InChI
InChI=1S/ClH.Na/h1H;/q;+1/p-1
2.1.3 InChI Key
FAPWRFPIFSIZLT-UHFFFAOYSA-M
2.1.4 Canonical SMILES
[Na+].[Cl-]
2.2 Other Identifiers
2.2.1 UNII
451W47IQ8X
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Sodium Chloride, (22)na

2. Sodium Chloride, (24)nacl

2.3.2 Depositor-Supplied Synonyms

1. 7647-14-5

2. Salt

3. Table Salt

4. Halite

5. Saline

6. Rock Salt

7. Common Salt

8. Dendritis

9. Purex

10. Sodium Chloric

11. Iodized Salt

12. Top Flake

13. Sodium Chloride (nacl)

14. Hyposaline

15. Sodium Monochloride

16. Flexivial

17. Gingivyl

18. Slow Sodium

19. Sea Salt

20. Nacl

21. Ss Salt

22. Sodiumchloride

23. Natriumchlorid

24. Adsorbanac

25. Hypersal

26. Sodium;chloride

27. Trisodium Trichloride

28. White Crystal

29. H.g. Blending

30. Salt (ingredient)

31. Colyte

32. Isotonic Saline

33. Sodium Chloride (na4cl4)

34. Caswell No. 754

35. Normal Saline

36. Natrum Muriaticum

37. Extra Fine 200 Salt

38. Extra Fine 325 Salt

39. Sodium Chloride Brine, Purified

40. Arm-a-vial

41. Ccris 982

42. Dendritic Salt

43. Hsdb 6368

44. Epa Pesticide Chemical Code 013905

45. 14762-51-7

46. Sodium Chloride Solution

47. Mfcd00003477

48. Nsc-77364

49. Sodium Chloride, Hypertonic

50. Ls-1700

51. 10% Sodium Chloride Injection

52. Chebi:26710

53. 451w47iq8x

54. Ayr

55. Buffer Solution, Tisab

56. Sodium Chloride, Ultra Dry

57. Sodium Chloride Solution, 5 M

58. Natriumchlorid [german]

59. Broncho Saline

60. Sodium, Reference Standard Solution

61. Halite (nacl)

62. Sodium Chloride, Acs Reagent, >=99.0%

63. Sodium-36 Chloride

64. Einecs 231-598-3

65. Nsc 77364

66. Sodium Chloride Physiological Solution, Bioultra, Tablet

67. Sodium Chloride (na36cl)

68. Sodium Chloride [usp:jan]

69. Isotonic

70. Kochsalz

71. Mafiron

72. Rocksalt

73. Titrisol

74. Cloruro Sodico

75. Sodium-chloride

76. Solsel

77. Unii-451w47iq8x

78. Natrii Chloridum

79. Saline Solution

80. Sea Water

81. Watesal A

82. Uzushio Biryuu M

83. Chlorure De Sodium

84. Adsorbanac (tn)

85. Brinewate Superfine

86. Sodium Chloride In Plastic Container

87. Sodium Chloride Salt

88. Canners 999

89. Sodium Chloride Acs

90. Nacl Solution, 1m

91. 0.9% Saline

92. Sodium Chloride 3% In Plastic Container

93. Sodium Chloride 5% In Plastic Container

94. Suprasel Nitrite

95. 0.9% Saline Solution

96. Saline, Sodium Chloride

97. Sodium Chloride, Tablet

98. Sodium Chloride (8ci)

99. Sodium Chloride 0.9% In Plastic Container

100. Mono-sodium Chloride Salt

101. 0.9% Nacl

102. Sodium Chloride 0.45% In Plastic Container

103. Sodium Chloride 23.4% In Plastic Container

104. Sodium Chloride, Isotonic

105. Unii-vr5y7pdt5w

106. Salt (6ci,7ci)

107. Vr5y7pdt5w

108. Special Salt 100/95

109. Nacl 0.9%

110. Wln: Na G

111. Ec 231-598-3

112. Sodium Chloride [ii]

113. Sodium Chloride [mi]

114. Sodium Chloride 0.9% In Sterile Plastic Container

115. Sodium Chloride, Acs Reagent

116. B1655 [langual]

117. Sodium Chloride [jan]

118. Rns60 Component Saline

119. Sodium Chloride (jp17/usp)

120. Sodium Chloride [hsdb]

121. Sodium Chloride [inci]

122. Sodium Chloride Solution, 1 M

123. Sodium Chloride Solution, 2 M

124. Sodium Chloride, Optical Grade

125. Sodium Chloride [vandf]

126. Sodium Chloride Anhydrous

127. Bacteriostatic Sodium Chloride 0.9% In Plastic Container

128. Chembl1200574

129. Dtxsid3021271

130. Natrum Muriaticum [hpus]

131. Rns-60 Component Saline

132. Sodium Chloride Biochemical Grade

133. 7647-14-5 (solid)

134. Sodium Chloride [usp-rs]

135. Sodium Chloride [who-dd]

136. Sodium Chloride [who-ip]

137. Sodium Chloride, Anhydrous

138. Sodium Chloride Solution, 0.1 M

139. Sodium Chloride Solution, 0.85%

140. Sodium Chloride Solution, Isotonic

141. Nsc77364

142. Sodium Chloride, Ar, >=99.9%

143. Sodium Chloride, Lr, >=99.5%

144. Sodium Chloride, Spectroscopy Grade

145. Str02627

146. Sodium Chloride, Manac Incorporated

147. Sodium Chloride [green Book]

148. Sodium Chloride, >=99%, Ar Grade

149. Sodium Chloride [orange Book]

150. Akos024438089

151. Akos024457457

152. Sodium Chloride [ep Monograph]

153. Sodium Chloride, Bacteriostatic

154. 10% Sodium Chloride Solution In Water

155. Db09153

156. Sodium Chloride [usp Monograph]

157. Sodium Chloride Saturated Solution 26%

158. Sodium Chloride, Technical Grade, 95%

159. Sodium Chloride, Technical Grade, 97%

160. Natrii Chloridum [who-ip Latin]

161. Sodium Chloride, Ph. Eur., Usp Grade

162. Sodium Chloride, P.a., 99-100.5%

163. 32343-72-9

164. Chloride Standard Solution, 1 Mg/ml Cl-

165. Sodium Chloride, Nist(r) Srm(r) 919b

166. Sodium Chloride, Reagentplus(r), >=99%

167. Sodium Chloride, Usp, 99.0-100.5%

168. Sodium Chloride, Usp, 99.0-101.0%

169. B7288

170. Ft-0645114

171. Q2314

172. S0572

173. Sodium Chloride, 0.1n Standardized Solution

174. Sodium Chloride, Bioxtra, >=99.5% (at)

175. Sodium Chloride, Saj First Grade, >=99.0%

176. Sodium Chloride, Tested According To Ph.eur.

177. D02056

178. Sodium Chloride, 99.999% Trace Metals Basis

179. Sodium Chloride, Jis Special Grade, >=99.5%

180. Sodium Chloride, Trace Metals Grade, 99.99%

181. Isotopic Standard For Chlorine, Nist Srm 975a

182. Sodium Chloride, 5m Aqueous Solution, Autoclaved

183. Sodium Chloride, Vetec(tm) Reagent Grade, 99%

184. Sodanylium And Hydrochloric Acid, Ion(1-) (1:1)

185. Sodium Chloride, 5m Aqueous Solution, Rnase Free

186. Sodium Chloride, Puriss. P.a., >=99.5% (at)

187. Sodium Chloride, Nist(r) Srm(r) 2201, Ion-selective

188. Sodium Chloride Crystal Optic Disc, 13mm X 2mm, Unpolished

189. Sodium Chloride Crystal Optic Disc, 25mm X 5mm, Unpolished

190. Sodium Chloride Crystal Optic Disc, 32mm X 3mm, Unpolished

191. Sodium Chloride, 5m Aqueous Solution, Ph 8.0, Autoclaved

192. Sodium Chloride Crystal Optic Disc, 13mm X 1mm, Polished Both Sides

193. Sodium Chloride Crystal Optic Disc, 13mm X 2mm, Polished Both Sides

194. Sodium Chloride Crystal Optic Disc, 22mm X 4mm, Polished Both Sides

195. Sodium Chloride Crystal Optic Disc, 25mm X 2mm, Polished Both Sides

196. Sodium Chloride Crystal Optic Disc, 25mm X 4mm, Polished Both Sides

197. Sodium Chloride Crystal Optic Disc, 32mm X 3mm, Polished Both Sides

198. Sodium Chloride Crystal Optic Disc, 38mm X 6mm, Polished Both Sides

199. Sodium Chloride, Bioultra, For Molecular Biology, >=99.5% (at)

200. Sodium Chloride, Puriss. P.a., >=99.5% (at), Powder Or Crystals

201. Sodium Chloride, Reagent Grade, >=98%, +80 Mesh Particle Size

202. Sodium Chloride, United States Pharmacopeia (usp) Reference Standard

203. Sodium Standard For Aas, Ready-to-use, Traceable To Bam, In H2o

204. Sodium Chloride Crystal Optic Rectangle, 30mm X 15mm X 4mm, Unpolished

205. Sodium Chloride Crystal Optic Rectangle, 38.5mm X 19.5mm X 4mm, Unpolished

206. Sodium Chloride Crystal Optic Rectangle, 41mm X 23mm X 6mm, Unpolished

207. Sodium Chloride Solution, Bioultra, For Molecular Biology, ~5 M In H2o

208. Sodium Chloride Solution, Technical, ~26% (saturated In Water At 20c, At)

209. Sodium Chloride, Anhydrous, Beads, -10 Mesh, 99.99% Trace Metals Basis

210. Sodium Chloride, Anhydrous, Beads, -10 Mesh, 99.999% Trace Metals Basis

211. Sodium Chloride, P.a., Acs Reagent, Reag. Iso, Reag. Ph. Eur., 99.5%

212. Sodium Chloride, Random Crystals, Optical Grade, 99.98% Trace Metals Basis

213. Sodium Chloride Crystal Optic Disc, 32mm X 3mm (drilled), Polished Both Sides

214. Sodium Chloride Crystal Optic Rectangle, 30mm X 15mm X 4mm (drilled), Polished Both Sides

215. Sodium Chloride Crystal Optic Rectangle, 30mm X 15mm X 4mm, Polished Both Sides

216. Sodium Chloride Crystal Optic Rectangle, 38.5mm X 19.5mm X 4mm, Polished Both Sides

217. Sodium Chloride Solution, 0.9% In Water, Bioxtra, Suitable For Cell Culture

218. Sodium Chloride, Anhydrous, Free-flowing, Redi-dri(tm), Reagentplus(r), >=99%

219. Sodium Chloride, Anhydrous, Redi-dri(tm), Free-flowing, Acs Reagent, >=99%

220. Sodium Chloride, Bioperformance Certified, >=99% (titration), Cell Culture Tested

221. Sodium Chloride, Meets Analytical Specification Of Ph. Eur., Bp, Usp, 99.0-100.5%

222. Sodium Chloride, Pharmaceutical Secondary Standard; Certified Reference Material

223. Sodium Chloride, Puriss. P.a., Acs Reagent, Reag. Iso, Reag. Ph. Eur., >=99.5%

224. Sodium Atomic Spectroscopy Standard Concentrate 1.00 G Na, 1.00 G/l, For 1 L Standard Solution, Analytical Standard

225. Sodium Atomic Spectroscopy Standard Concentrate 10.00 G Na, 10.00 G/l, For 1 L Standard Solution, Analytical Standard

226. Sodium Chloride Crystal Optic Rectangle, 38.5mm X 19.5mm X 4mm (drilled), Polished Both Sides

227. Sodium Chloride Solution, 5 M In H2o, Bioreagent, For Molecular Biology, Suitable For Cell Culture

228. Sodium Chloride, Bioreagent, Suitable For Cell Culture, Suitable For Insect Cell Culture, Suitable For Plant Cell Culture, >=99%

229. Sodium Chloride, Certified Reference Material For Titrimetry, Certified By Bam, According To Iso 17025, >=99.5%

230. Sodium Chloride, For Molecular Biology, Dnase, Rnase, And Protease, None Detected, >=98% (titration)

231. Sodium Chloride, Pharmagrade, Usp, Manufactured Under Appropriate Gmp Controls For Pharma Or Biopharmaceutical Production.

232. Sodium Chloride, Puriss., Meets Analytical Specification Of Ph. Eur., Bp, Usp, 99.0-100.5% (calc. To The Dried Substance), <=0.00002% Al

233. Sodium Standard Solution, Suitable For Atomic Absorption Spectrometry, 1000 Ppm Na, 1 Mg/ml Na

2.4 Create Date
2005-03-25
3 Chemical and Physical Properties
Molecular Weight 58.44 g/mol
Molecular Formula ClNa
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass57.9586220 g/mol
Monoisotopic Mass57.9586220 g/mol
Topological Polar Surface Area0 Ų
Heavy Atom Count2
Formal Charge0
Complexity2
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Drug Information
1 of 6  
Drug NameBroncho saline
PubMed HealthSodium Chloride (By breathing)
Drug ClassesAntiasthma, Respiratory Agent
Drug Label14.6% Sodium Chloride Injection, USP Additive Solution is a sterile, nonpyrogenic, concentrated solution for intravenous administration ONLY AFTER DILUTION to replenish electrolytes. The preparations contain either 2.92 or 5.84 g of sodium chloride (...
Active IngredientSodium chloride
Dosage FormAerosol, metered
RouteInhalation
Strength0.9%
Market StatusOver the Counter
CompanyBlairex

2 of 6  
Drug NameSodium chloride
PubMed HealthSodium Chloride
Drug ClassesAntiasthma, Osmotherapy Agent, Parenteral Electrolyte, Sodium, Respiratory Agent, Sodium Supplement
Active IngredientSodium chloride
Dosage FormInjectable
Routeinjection
Strength10ml
Market StatusPrescription
CompanyTaro Pharms Ireland

3 of 6  
Drug NameSodium chloride in plastic container
Active IngredientSodium chloride
Dosage FormInjectable
RouteInjection
Strength2.5meq/ml
Market StatusPrescription
CompanyHospira

4 of 6  
Drug NameBroncho saline
PubMed HealthSodium Chloride (By breathing)
Drug ClassesAntiasthma, Respiratory Agent
Drug Label14.6% Sodium Chloride Injection, USP Additive Solution is a sterile, nonpyrogenic, concentrated solution for intravenous administration ONLY AFTER DILUTION to replenish electrolytes. The preparations contain either 2.92 or 5.84 g of sodium chloride (...
Active IngredientSodium chloride
Dosage FormAerosol, metered
RouteInhalation
Strength0.9%
Market StatusOver the Counter
CompanyBlairex

5 of 6  
Drug NameSodium chloride
PubMed HealthSodium Chloride
Drug ClassesAntiasthma, Osmotherapy Agent, Parenteral Electrolyte, Sodium, Respiratory Agent, Sodium Supplement
Active IngredientSodium chloride
Dosage FormInjectable
Routeinjection
Strength10ml
Market StatusPrescription
CompanyTaro Pharms Ireland

6 of 6  
Drug NameSodium chloride in plastic container
Active IngredientSodium chloride
Dosage FormInjectable
RouteInjection
Strength2.5meq/ml
Market StatusPrescription
CompanyHospira

4.2 Therapeutic Uses

Sodium chloride injections are used as a source of sodium chloride and water for hydration. Sodium chloride is used in the prevention or treatment of deficiencies of sodium and chloride ions and in the prevention of muscle cramps and heat prostration resulting from excessive perspiration during exposure to high temperature. Sodium chloride is also used to treat deficiencies of sodium and chloride caused by excessive diuresis or excessive salt restriction.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 2758


0.45% Sodium chloride injection is used principally as a hydrating solution and may be used to assess renal function status, since more water is provided than is required for excretion of salt. 0.45% Sodium chloride injection is also used in the management of hyperosmolar diabetes.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 2758


0.9% Sodium chloride injection is used for extracellular fluid replacement and in the management of metabolic alkalosis in the presence of fluid loss and mild sodium depletion. 0.9% Sodium chloride injection (normal saline) is also used as a priming fluid for hemodialysis procedures and to initiate and terminate blood transfusions.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 2758


Hypertonic (i.e., 3%, 5%) sodium chloride injection is used in the management of severe sodium chloride depletion when rapid electrolyte restoration is essential. Severe sodium chloride depletion may occur in the presence of heart failure or renal impairment, or during surgery or postoperatively. In these conditions, chloride loss often exceeds sodium loss. Hypertonic sodium chloride injections are also used in the management of hyponatremia and hypochloremia resulting from administration of sodium-free fluids during fluid and electrolyte therapy; in the management of extreme dilution of extracellular fluid following excessive water intake (e.g., that resulting from multiple enemas or perfusion of irrigating solutions into open venous sinuses during transurethral prostatic resections); and in the emergency treatment of severe sodium chloride depletion resulting from excess sweating, vomiting, diarrhea, and other conditions.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 2758


For more Therapeutic Uses (Complete) data for SODIUM CHLORIDE (13 total), please visit the HSDB record page.


4.3 Drug Warning

Bacteriostatic sodium chloride injection containing benzyl alcohol as a preservative (antimicrobial agent) should not be used for diluting or reconstituting drugs for administration in neonates nor should it be used to flush intravascular catheters in neonates. Several deaths have been reported in neonates weighing less than 2.5 kg in whom bacteriostatic sodium chloride for injection containing 0.9% benzyl alcohol was used for flushing IV catheters; some of these neonates received additional benzyl alcohol when bacteriostatic sodium chloride injection was used to dilute or reconstitute drugs. The deaths were usually preceded by a syndrome that included metabolic acidosis, CNS depression, respiratory distress progressing to gasping respiration, hypotension, renal failure, and, occasionally, seizures and intracranial hemorrhage. High concentrations of benzyl alcohol, benzoic acid, and hippuric acid (a metabolite) were present in blood and urine in these neonates. Benzyl alcohol toxicity apparently was caused by administration of relatively large daily doses (99-404 mg/kg daily) of the preservative in proportion to the neonate's weight. Although these neonates had biochemical evidence of benzyl alcohol toxicity, they also had serious underlying conditions.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 2759


Sodium chloride is contraindicated in patients with conditions in which administration of sodium and chloride is detrimental. Sodium chloride 3 and 5% injections are also contraindicated in the presence of increased, normal, or only slightly decreased serum electrolyte concentrations.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 2759


Sodium chloride should be used with extreme caution, if at all, in patients with congestive heart failure or other edematous or sodium-retaining conditions, in patients with severe renal insufficiency, in patients with liver cirrhosis, and in patients receiving corticosteroids or corticotropin; particular caution is necessary in geriatric or postoperative patients. IV administration of sodium chloride may cause fluid and/or solute overload resulting in dilution of serum electrolytes, overhydration, congestive conditions, or pulmonary edema. The risk of dilutional conditions is inversely proportional to the electrolyte concentration administered, and the risk of solute overload and resultant congestive conditions with peripheral and/or pulmonary edema is directly proportional to the electrolyte concentration administered. The manufacturers warn that excessive IV administration of sodium chloride may result in hypokalemia.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 2759


Changes in fluid balance, electrolyte concentrations, and acid-base balance should be evaluated clinically and via periodic laboratory determinations during prolonged therapy with sodium chloride and in patients whose condition warrants such evaluation. Substantial changes may require additional electrolyte supplements or other appropriate therapy. Additional electrolyte supplementation may also be required in patients with substantial electrolyte losses resulting from conditions such as protracted nasogastric suctioning, vomiting, diarrhea, or GI fistula drainage.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 2759


For more Drug Warnings (Complete) data for SODIUM CHLORIDE (12 total), please visit the HSDB record page.


4.4 Minimum/Potential Fatal Human Dose

The estimated fatal dose of sodium chloride is approximately 0.75 to 3.00 g/kg.

Dart, R.C. (ed). Medical Toxicology. Third Edition, Lippincott Williams & Wilkins. Philadelphia, PA. 2004., p. 1057


An estimated dose of more than 400 mEq/kg resulted in brain injury and death in a 2 year old child given a salt water solution to induce emesis.

Dart, R.C. (ed). Medical Toxicology. Third Edition, Lippincott Williams & Wilkins. Philadelphia, PA. 2004., p. 1057


4.5 Drug Indication

This intravenous solution is indicated for use in adults and pediatric patients as a source of electrolytes and water for hydration. Also, designed for use as a diluent and delivery system for intermittent intravenous administration of compatible drug additives.


5 Pharmacology and Biochemistry
5.1 Pharmacology

Sodium, the major cation of the extracellular fluid, functions primarily in the control of water distribution, fluid balance, and osmotic pressure of body fluids. Sodium is also associated with chloride and bicarbonate in the regulation of the acid-base equilibrium of body fluid. Chloride, the major extracellular anion, closely follows the metabolism of sodium, and changes in the acid-base balance of the body are reflected by changes in the chloride concentration.


5.2 FDA Pharmacological Classification
5.2.1 Pharmacological Classes
Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Increased Large Intestinal Motility [PE]
5.3 ATC Code

A - Alimentary tract and metabolism

A12 - Mineral supplements

A12C - Other mineral supplements

A12CA - Sodium

A12CA01 - Sodium chloride


B - Blood and blood forming organs

B05 - Blood substitutes and perfusion solutions

B05C - Irrigating solutions

B05CB - Salt solutions

B05CB01 - Sodium chloride


B - Blood and blood forming organs

B05 - Blood substitutes and perfusion solutions

B05X - I.v. solution additives

B05XA - Electrolyte solutions

B05XA03 - Sodium chloride


S - Sensory organs

S01 - Ophthalmologicals

S01X - Other ophthalmologicals

S01XA - Other ophthalmologicals

S01XA03 - Sodium chloride, hypertonic


5.4 Absorption, Distribution and Excretion

Absorption

Absorption of sodium in the small intestine plays an important role in the absorption of chloride, amino acids, glucose, and water. Chloride, in the form of hydrochloric acid (HCl), is also an important component of gastric juice, which aids the digestion and absorption of many nutrients.


Route of Elimination

Substantially excreted by the kidneys.


Volume of Distribution

The volume of distribution is 0.64 L/kg.


The primary route of sodium excretion is the urine; additional excretion occurs in sweat and feces. The kidney filters sodium a the glomerulus, but 60% to 70% is reabsorbed in the proximal tubules along with bicarbonate and water. Another 25% to 30% is reabsorbed in the loop of Henle, along with chloride and water. In the distal tubules, aldosterone modulates the reabsorption of sodium and, indirectly, chloride. The renal threshold for sodium is 110 to 130 mEq/L. Less than 1% of the filtered sodium is excreted in the urine.

Dart, R.C. (ed). Medical Toxicology. Third Edition, Lippincott Williams & Wilkins. Philadelphia, PA. 2004., p. 1057


Sodium is rapidly absorbed from the GI tract; it is also absorbed from rectal enemas. Intestinal wall absorption occurs via the Na+, K+-adenosine triphosphatase system that is augmented by aldosterone and desoxycorticosterone acetate. Sodium is not bound by plasma proteins. The volume of distribution is 0.64 L/kg.

Dart, R.C. (ed). Medical Toxicology. Third Edition, Lippincott Williams & Wilkins. Philadelphia, PA. 2004., p. 1057


In one study using radiolabeled 20% sodium chloride injection, most of the drug concentrated in the decidua and the fetal part of the placenta following intra-amniotic injection. Following intra-amniotic administration of 20% sodium chloride injection, some of the drug diffuses into the maternal blood.

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 3323


Atrichial sweat glands ... are the organs by which considerable body water and electrolytes, mainly sodium chloride, are lost.

Bingham, E.; Cohrssen, B.; Powell, C.H.; Patty's Toxicology Volumes 1-9 5th ed. John Wiley & Sons. New York, N.Y. (2001)., p. 8:69


For more Absorption, Distribution and Excretion (Complete) data for SODIUM CHLORIDE (6 total), please visit the HSDB record page.


5.5 Metabolism/Metabolites

The salt that is taken in to gastro intestinal tract remains for the most part unabsorbed as the liquid contents pass through the stomach and small bowel. On reaching the colon this salt, together with the water is taken in to the blood. As excesses are absorbed the kidney is constantly excreting sodium chloride, so that the chloride level in the blood and tissues remains fairly constant.Further more, if the chloride intake ceases, the kidney ceases to excrete chlorides. Body maintains an equilibrium retaining the 300gm of salt dissolved in the blood and fluid elements of the tissue dissociated into sodium ions and chloride ions.


5.6 Biological Half-Life

17 minutes


5.7 Mechanism of Action

Sodium and chloride major electrolytes of the fluid compartment outside of cells (i.e., extracellular) work together to control extracellular volume and blood pressure. Disturbances in sodium concentrations in the extracellular fluid are associated with disorders of water balance.


Intra-amniotic instillation of 20% sodium chloride injection induces abortion and fetal death. Although the mechanism has not been conclusively determined, some studies indicate that the drug's abortifacient activity may be mediated by prostaglandins released from decidual cells damaged by hypertonic solutions of sodium chloride. Hypertonic sodium chloride-induced uterine contractions are usually sufficient to cause evacuation of both the fetus and placenta; however, abortion may be incomplete in 25-40% of patients. /20% injection/

American Society of Health-System Pharmacists 2013; Drug Information 2013. Bethesda, MD. 2013, p. 3323


FDA Orange Book

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  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Flag India
Digital Content Digital Content

RLD : No

TE Code : AA

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

Brand Name : POLYETHYLENE GLYCOL 3350 AND ELECTROLYTES

Dosage Form : FOR SOLUTION;ORAL

Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

Approval Date : 2018-12-21

Application Number : 204558

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

Strides Pharma Science

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

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Digital Content Digital Content

RLD : No

TE Code : AA

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

Brand Name : PEG-3350, POTASSIUM CHLORIDE, SODIUM BICARBONATE, SODIUM CHLORIDE

Dosage Form : FOR SOLUTION;ORAL

Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

Approval Date : 2015-04-13

Application Number : 204559

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

Strides Pharma Science

03

GOLDLINE

Israel
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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Digital Content Digital Content

RLD : No

TE Code :

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

Brand Name : GLYCOPREP

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

Approval Date : 1988-12-23

Application Number : 72319

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

TAPI Company Banner

04

ABBOTT

U.S.A
RDD
Not Confirmed
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ABBOTT

U.S.A
arrow
RDD
Not Confirmed

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Brand Name : AMINOSYN II 4.25% W/ ELECTROLYTES IN DEXTROSE 25% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 4.25%;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date : 1986-12-16

Application Number : 19564

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

RDD
Not Confirmed
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RDD
Not Confirmed

SODIUM CHLORIDE

Brand Name : BACTERIOSTATIC SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INJECTION

Dosage Strength : 90MG/10ML (9MG/ML)

Approval Date : 1985-05-15

Application Number : 88909

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

B BRAUN

U.S.A
RDD
Not Confirmed
arrow

B BRAUN

U.S.A
arrow
RDD
Not Confirmed

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Brand Name : DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.30% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5GM/100ML;300MG/100ML;330MG/100ML

Approval Date : 1986-01-18

Application Number : 18268

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

B BRAUN

U.S.A
RDD
Not Confirmed
arrow

B BRAUN

U.S.A
arrow
RDD
Not Confirmed

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Brand Name : POTASSIUM CHLORIDE 0.11% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10GM/100ML;110MG/100ML;900MG/100ML

Approval Date : 1988-02-17

Application Number : 19630

RX/OTC/DISCN : RX

RLD : No

TE Code :

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08

RDD
Not Confirmed
arrow
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RDD
Not Confirmed

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Brand Name : POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5GM/100ML;150MG/100ML;900MG/100ML

Approval Date : 1985-04-05

Application Number : 19308

RX/OTC/DISCN : RX

RLD : No

TE Code :

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09

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE

Brand Name : TRAVASOL 4.25% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 25% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 4.25%;25GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date : 1995-10-23

Application Number : 20147

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

BRAINTREE

U.S.A
RDD
Not Confirmed
arrow

BRAINTREE

U.S.A
arrow
RDD
Not Confirmed

BISACODYL; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

Brand Name : HALFLYTELY

Dosage Form : FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL

Dosage Strength : 5MG,N/A;N/A,210GM;N/A,0.74GM;N/A,2.86GM;N/A,5.6GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2010-07-16

Application Number : 21551

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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Europe

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01

Helvepharm Ag

France
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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Digital Content Digital Content

Regulatory Info : Allowed

Registration Country : Switzerland

Glucose; Sodium Chloride; Potassium Chloride; Sodium Citrate Dihydrate

Brand Name : Elotrans

Dosage Form : Powder For Oral Solution

Dosage Strength :

Packaging :

Approval Date : 17/03/1983

Application Number : 44644

Regulatory Info : Allowed

Registration Country : Switzerland

Sanofi Company Banner

02

Glucose (Anhydrous); Potassium Chloride; Sodium Citrate (Dihydrate); Sodium Chloride

Brand Name : Aqurex

Dosage Form : Powder For Oral Solution

Dosage Strength :

Packaging :

Approval Date : 28-06-2012

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

Fermion Orion Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Flag India
Digital Content Digital Content

Regulatory Info : Prescription

Registration Country : Denmark

Potassium Chloride; Macrogol 3350; Sodium Chloride; Sodium Hydrogen Carbonate

Brand Name : Sacrovic

Dosage Form : Powder For Oral Solution

Dosage Strength :

Packaging :

Approval Date : 11-06-2024

Application Number : 28106990923

Regulatory Info : Prescription

Registration Country : Denmark

Strides Pharma Science

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Flag India
Digital Content Digital Content

Regulatory Info : Prescription

Registration Country : Denmark

Potassium Chloride; Macrogol 3350; Sodium Chloride; Sodium Hydrogen Carbonate

Brand Name : Sacrovic Junior

Dosage Form : Powder For Oral Solution

Dosage Strength :

Packaging :

Approval Date : 11-06-2024

Application Number : 28106990523

Regulatory Info : Prescription

Registration Country : Denmark

Strides Pharma Science

05

RDD
Not Confirmed
arrow
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RDD
Not Confirmed

Sodium Chloride

Brand Name : Sodium Chloride

Dosage Form : Sodium Chloride 0.9% 2Ml Parenteral Use

Dosage Strength : 1 Vial 2 ml 0.9%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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06

RDD
Not Confirmed
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RDD
Not Confirmed

Sodium Chloride

Brand Name : Sodium Chloride

Dosage Form : Sodium Chloride 0.9% 5Ml Parenteral Use

Dosage Strength : 1 Vial 5 ml 0.9%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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07

RDD
Not Confirmed
arrow
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RDD
Not Confirmed

Sodium Chloride

Brand Name :

Dosage Form : NASAL SPRAY

Dosage Strength : 0.704%

Packaging : 30 Ml/Bottle

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : Turkey

blank

08

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

Sodium Chloride

Brand Name :

Dosage Form : NASAL SPRAY

Dosage Strength : 0.9%

Packaging : 30 Ml/Bottle

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : Turkey

blank

09

SALF SpA

Country
RDD
Not Confirmed
arrow

SALF SpA

Country
arrow
RDD
Not Confirmed

Sodium Chloride

Brand Name : Sodium Chloride

Dosage Form : Sodium Chloride 0.9% 2Ml Parenteral Use

Dosage Strength : 1 Vial 2 ml 0.9%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

blank

10

MONICO SpA

Country
RDD
Not Confirmed
arrow

MONICO SpA

Country
arrow
RDD
Not Confirmed

Sodium Chloride

Brand Name : Sodium Chloride

Dosage Form : Sodium Chloride 0.9% 2Ml Parenteral Use

Dosage Strength : 1 Vial 2 ml 0.9%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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DRUG PRODUCT COMPOSITIONS

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DOSAGE - INJECTABLE;INJECTION - 900MG/100ML

USFDA APPLICATION NUMBER - 16366

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DOSAGE - SOLUTION;INJECTION - 225MG/25ML (9MG...DOSAGE - SOLUTION;INJECTION - 225MG/25ML (9MG/ML)

USFDA APPLICATION NUMBER - 16677

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DOSAGE - SOLUTION;INJECTION - 450MG/50ML (9MG...DOSAGE - SOLUTION;INJECTION - 450MG/50ML (9MG/ML)

USFDA APPLICATION NUMBER - 16677

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DOSAGE - SOLUTION;INJECTION - 900MG/100ML

USFDA APPLICATION NUMBER - 16677

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DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;30...DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML

USFDA APPLICATION NUMBER - 16682

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DOSAGE - SOLUTION;IRRIGATION - 900MG/100ML

USFDA APPLICATION NUMBER - 16733

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 17512

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 17512

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/100ML;3.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 17512

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 17512

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 17512

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 17512

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;3.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 17512

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 17512

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DOSAGE - SOLUTION;IRRIGATION - 900MG/100ML

USFDA APPLICATION NUMBER - 17514

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;900...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;900MG/100ML

USFDA APPLICATION NUMBER - 17585

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;225...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;225MG/100ML

USFDA APPLICATION NUMBER - 17606

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;450...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;450MG/100ML

USFDA APPLICATION NUMBER - 17607

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DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5G...DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML

USFDA APPLICATION NUMBER - 17608

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;300...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;300MG/100ML

USFDA APPLICATION NUMBER - 17799

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DOSAGE - INJECTABLE;INJECTION - 450MG/100ML

USFDA APPLICATION NUMBER - 18016

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DOSAGE - INJECTABLE;INJECTION - 450MG/100ML

USFDA APPLICATION NUMBER - 18090

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;149...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;149MG/100ML;450MG/100ML

USFDA APPLICATION NUMBER - 18362

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;224...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;224MG/100ML;450MG/100ML

USFDA APPLICATION NUMBER - 18362

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;298...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;298MG/100ML;450MG/100ML

USFDA APPLICATION NUMBER - 18362

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;74....DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;74.5MG/100ML;450MG/100ML

USFDA APPLICATION NUMBER - 18362

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;149...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;149MG/100ML;225MG/100ML

USFDA APPLICATION NUMBER - 18365

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;298...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;298MG/100ML;225MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 18365

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;74....DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;74.5MG/100ML;225MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 18365

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DOSAGE - SOLUTION;IRRIGATION - 0.154MG/ML;0.9...DOSAGE - SOLUTION;IRRIGATION - 0.154MG/ML;0.92MG/ML;0.184MG/ML;0.2MG/ML;0.38MG/ML;2.1MG/ML;7.14MG/ML;0.42MG/ML

USFDA APPLICATION NUMBER - 18469

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DOSAGE - SOLUTION;INJECTION - 180MG/20ML (9MG...DOSAGE - SOLUTION;INJECTION - 180MG/20ML (9MG/ML)

USFDA APPLICATION NUMBER - 18800

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DOSAGE - SOLUTION;INJECTION - 270MG/30ML (9MG...DOSAGE - SOLUTION;INJECTION - 270MG/30ML (9MG/ML)

USFDA APPLICATION NUMBER - 18800

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DOSAGE - SOLUTION;INJECTION - 90MG/10ML (9MG/...DOSAGE - SOLUTION;INJECTION - 90MG/10ML (9MG/ML)

USFDA APPLICATION NUMBER - 18800

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DOSAGE - SOLUTION;INJECTION - 180MG/20ML (9MG...DOSAGE - SOLUTION;INJECTION - 180MG/20ML (9MG/ML)

USFDA APPLICATION NUMBER - 18803

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DOSAGE - SOLUTION;INJECTION - 18MG/2ML (9MG/M...DOSAGE - SOLUTION;INJECTION - 18MG/2ML (9MG/ML)

USFDA APPLICATION NUMBER - 18803

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DOSAGE - SOLUTION;INJECTION - 27MG/3ML (9MG/M...DOSAGE - SOLUTION;INJECTION - 27MG/3ML (9MG/ML)

USFDA APPLICATION NUMBER - 18803

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DOSAGE - SOLUTION;INJECTION - 450MG/50ML (9MG...DOSAGE - SOLUTION;INJECTION - 450MG/50ML (9MG/ML)

USFDA APPLICATION NUMBER - 18803

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DOSAGE - SOLUTION;INJECTION - 45MG/5ML (9MG/M...DOSAGE - SOLUTION;INJECTION - 45MG/5ML (9MG/ML)

USFDA APPLICATION NUMBER - 18803

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DOSAGE - SOLUTION;INJECTION - 90MG/10ML (9MG/...DOSAGE - SOLUTION;INJECTION - 90MG/10ML (9MG/ML)

USFDA APPLICATION NUMBER - 18803

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;1.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

USFDA APPLICATION NUMBER - 18883

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 18883

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;2.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

USFDA APPLICATION NUMBER - 18883

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 18883

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;4.25GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

USFDA APPLICATION NUMBER - 18883

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 18883

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DOSAGE - SOLUTION;IRRIGATION - 20MG/100ML;30M...DOSAGE - SOLUTION;IRRIGATION - 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML

USFDA APPLICATION NUMBER - 19416

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DOSAGE - INJECTABLE;INJECTION - 450MG/100ML

USFDA APPLICATION NUMBER - 19635

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DOSAGE - INJECTABLE;INJECTION - 900MG/100ML

USFDA APPLICATION NUMBER - 19635

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DOSAGE - SOLUTION;INJECTION - 90MG/10ML (9MG/...DOSAGE - SOLUTION;INJECTION - 90MG/10ML (9MG/ML)

USFDA APPLICATION NUMBER - 19635

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DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5G...DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;104MG/100ML;600MG/100ML;310MG/100ML

USFDA APPLICATION NUMBER - 19685

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DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5G...DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML

USFDA APPLICATION NUMBER - 19685

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DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5G...DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML

USFDA APPLICATION NUMBER - 19685

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DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5G...DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML

USFDA APPLICATION NUMBER - 19685

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;149...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;149MG/100ML;900MG/100ML

USFDA APPLICATION NUMBER - 19691

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;224...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;224MG/100ML;900MG/100ML

USFDA APPLICATION NUMBER - 19691

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;298...DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;298MG/100ML;900MG/100ML

USFDA APPLICATION NUMBER - 19691

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DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;74....DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;74.5MG/100ML;900MG/100ML

USFDA APPLICATION NUMBER - 19691

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DOSAGE - FOR SOLUTION;ORAL - 420GM/BOT;1.48GM...DOSAGE - FOR SOLUTION;ORAL - 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

USFDA APPLICATION NUMBER - 19797

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20163

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20163

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DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20163

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.4MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.4MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20171

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.4MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.4MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20171

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.4MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.4MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20171

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20183

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20183

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/100ML;3.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20183

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DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/10...DOSAGE - SOLUTION;INTRAPERITONEAL - 18.3MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

USFDA APPLICATION NUMBER - 20183

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DOSAGE - INJECTABLE;INJECTION - 3.68GM/1000ML...DOSAGE - INJECTABLE;INJECTION - 3.68GM/1000ML;3.05GM/1000ML;0.314GM/1000ML ;3.09GM/1000ML;6.34GM/1000ML;0.187GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 207026

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DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;3....DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;3.05GM/1000ML;0.314GM/1000ML;2.21GM/1000ML;6.95GM/1000ML;0.187GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 207026

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DOSAGE - SOLUTION;IRRIGATION - 0.48MG/ML;0.3M...DOSAGE - SOLUTION;IRRIGATION - 0.48MG/ML;0.3MG/ML;0.75MG/ML;3.9MG/ML;6.4MG/ML;1.7MG/ML

USFDA APPLICATION NUMBER - 20742

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DOSAGE - INJECTABLE;INJECTION - 3.68GM/1000ML...DOSAGE - INJECTABLE;INJECTION - 3.68GM/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;0.314GM/1000ML;2.21GM/1000ML;7.07GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - 3.68GM/1000ML...DOSAGE - INJECTABLE;INJECTION - 3.68GM/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;0.314GM/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - 3.68GM/1000ML...DOSAGE - INJECTABLE;INJECTION - 3.68GM/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;N/A/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - 5.15GM/1000ML...DOSAGE - INJECTABLE;INJECTION - 5.15GM/1000ML;20GM/1000ML;5.4GM/1000ML;2.03GM/1000ML;0.157GM/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - 5.15GM/1000ML...DOSAGE - INJECTABLE;INJECTION - 5.15GM/1000ML;N/A/1000ML;5.4GM/1000ML;2.03GM/1000ML;N/A/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;20...DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;20GM/1000ML;5.4GM/1000ML;2.03GM/1000ML;0.157GM/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;20...DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;20GM/1000ML;5.4GM/1000ML;2.44GM/1000ML;0.314GM/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;20...DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;0.157GM/1000ML;2.21GM/1000ML;7.07GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;20...DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;0.314GM/1000ML;2.21GM/1000ML;7.07GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;N/...DOSAGE - INJECTABLE;INJECTION - N/A/1000ML;N/A/1000ML;5.4GM/1000ML;2.44GM/1000ML;N/A/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)

USFDA APPLICATION NUMBER - 21703

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01

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RDD
Not Confirmed
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RDD
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Company : B.Braun

Dextrose 10 % And 0.45 % NaCl

Drug Cost (USD) : 3,349

Year : 2023

Prescribers : 16

Prescriptions : 52

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02

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Company : Baxter Healthca

Dextrose 5 %-0.2 % Sod Chlorid

Drug Cost (USD) : 1,745

Year : 2023

Prescribers : 39

Prescriptions : 95

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03

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Company : B.Braun

Dextrose 5 %-0.45 % Sod Chlord

Drug Cost (USD) : 45,006

Year : 2023

Prescribers : 1424

Prescriptions : 2411

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04

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Company : Baxter Healthca

Dextrose 5 %-0.45 % Sod Chlord

Drug Cost (USD) : 459,570

Year : 2023

Prescribers : 12391

Prescriptions : 20853

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05

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Not Confirmed
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Company : Fresenius Kabi

Dextrose 5 %-0.45 % Sod Chlord

Drug Cost (USD) : 3,416

Year : 2023

Prescribers : 201

Prescriptions : 235

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06

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Not Confirmed
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Company : B.Braun

Dextrose 5 % And 0.9 % NaCl

Drug Cost (USD) : 23,009

Year : 2023

Prescribers : 533

Prescriptions : 937

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07

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Not Confirmed
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Company : Baxter Healthca

Dextrose 5 % And 0.9 % NaCl

Drug Cost (USD) : 147,867

Year : 2023

Prescribers : 3830

Prescriptions : 6253

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08

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Not Confirmed
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Company : Fresenius Kabi

Dextrose 5 % And 0.9 % NaCl

Drug Cost (USD) : 518

Year : 2023

Prescribers : 26

Prescriptions : 33

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09

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Not Confirmed
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Company : Gavis/Lupin

Sodium Chloride/NaHCO3/KCl/PEG

Drug Cost (USD) : 20,995

Year : 2023

Prescribers : 1053

Prescriptions : 1087

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10

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Not Confirmed
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Company : B.Braun

Potassium Chloride/D5-0.45NaCl

Drug Cost (USD) : 2,681

Year : 2023

Prescribers : 62

Prescriptions : 130

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01

Brand Name : Polyethylene Glycol + Salts ...

Italy
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RDD
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Brand Name : Polyethylene Glycol + Salts ...

Italy
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RDD
Not Confirmed

PEG-30 Dipolyhydroxy Stearate; Sodium Sulfate; Sodium Bicarbonate; Sodium Chloride; Potassium Chloride

Dosage Form :

Dosage Strength : 16 Bust Groun Os 17.5 G  

Price Per Pack (Euro) : 10

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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02

Brand Name : Freamine Iii 8,5%

Germany
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Not Confirmed

Brand Name : Freamine Iii 8,5%

Germany
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RDD
Not Confirmed

Sodium Acetate; Magnesium Acetate; Sodium Chloride; Potassium Chloride; Phosphoric Acid

Dosage Form :

Dosage Strength : 1 Bottle Ev 500 Ml  

Price Per Pack (Euro) : 11.22

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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03

Brand Name : Sodium Chloride

Country
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Not Confirmed

Brand Name : Sodium Chloride

Country
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RDD
Not Confirmed

Sodium Chloride

Dosage Form :

Dosage Strength : 1 Ampoule 2 Meq/Ml 10 Ml  

Price Per Pack (Euro) : 0.57

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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04

Brand Name : Re-Hydration Electrolytic Ii...

Country
arrow
RDD
Not Confirmed

Brand Name : Re-Hydration Electrolytic Ii...

Country
arrow
RDD
Not Confirmed

Sodium Chloride; Potassium Chloride; Calcium Chloride; Magnesium Chloride; Sodium Acetate; Sodium Citrate

Dosage Form :

Dosage Strength : 1 Bottle 1,000 Ml  

Price Per Pack (Euro) : 3.59

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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05

Brand Name : Re-Hydration Electrolytic Ii...

Country
arrow
RDD
Not Confirmed

Brand Name : Re-Hydration Electrolytic Ii...

Country
arrow
RDD
Not Confirmed

Sodium Chloride; Potassium Chloride; Calcium Chloride; Magnesium Chloride; Sodium Acetate; Sodium Citrate

Dosage Form :

Dosage Strength : 1 500 Ml Bottle  

Price Per Pack (Euro) : 2.47

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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06

Brand Name : Maintaining The Electrolytic...

Country
arrow
RDD
Not Confirmed

Brand Name : Maintaining The Electrolytic...

Country
arrow
RDD
Not Confirmed

Sodium Chloride; Potassium Chloride; Potassium Phosphate; Sodium Acetate

Dosage Form :

Dosage Strength : 1 Bottle 1,000 Ml  

Price Per Pack (Euro) : 3.59

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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07

Brand Name : Maintaining The Electrolytic...

Country
arrow
RDD
Not Confirmed

Brand Name : Maintaining The Electrolytic...

Country
arrow
RDD
Not Confirmed

Sodium Chloride; Potassium Chloride; Potassium Phosphate; Sodium Acetate

Dosage Form :

Dosage Strength : 1 500 Ml Bottle  

Price Per Pack (Euro) : 2.47

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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08

Brand Name : Re-Hydration Electrolytic I

Country
arrow
RDD
Not Confirmed

Brand Name : Re-Hydration Electrolytic I

Country
arrow
RDD
Not Confirmed

Lactic Acid; Sodium Hydroxide; Sodium Chloride; Potassium Chloride

Dosage Form :

Dosage Strength : 1 500 Ml Bottle  

Price Per Pack (Euro) : 2.11

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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09

Brand Name : Re-Hydration Electrolytic I

Country
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RDD
Not Confirmed

Brand Name : Re-Hydration Electrolytic I

Country
arrow
RDD
Not Confirmed

Lactic Acid; Sodium Hydroxide; Sodium Chloride; Potassium Chloride

Dosage Form :

Dosage Strength : 1 Bag 500 Ml  

Price Per Pack (Euro) : 2.21

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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10

Brand Name : Ringer Lactate

Country
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RDD
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Brand Name : Ringer Lactate

Country
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Lactic Acid; Sodium Hydroxide; Sodium Chloride; Potassium Chloride; Calcium Chloride

Dosage Form :

Dosage Strength : 1 Bag 1,000 Ml  

Price Per Pack (Euro) : 2.85

Published in :

Country : Italy

RX/OTC/DISCN : Class C

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ABOUT THIS PAGE

Looking for 7647-14-5 / Sodium Chloride API manufacturers, exporters & distributors?

Sodium Chloride manufacturers, exporters & distributors 1

55

PharmaCompass offers a list of Sodium Chloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Sodium Chloride manufacturer or Sodium Chloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Chloride manufacturer or Sodium Chloride supplier.

API | Excipient name

Sodium Chloride

Synonyms

7647-14-5, Salt, Table salt, Halite, Saline, Rock salt

Cas Number

7647-14-5

Unique Ingredient Identifier (UNII)

451W47IQ8X

About Sodium Chloride

A ubiquitous sodium salt that is commonly used to season food.

Sodium chloride USP crystal grade Manufacturers

A Sodium chloride USP crystal grade manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium chloride USP crystal grade, including repackagers and relabelers. The FDA regulates Sodium chloride USP crystal grade manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium chloride USP crystal grade API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Sodium chloride USP crystal grade manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.

Sodium chloride USP crystal grade Suppliers

A Sodium chloride USP crystal grade supplier is an individual or a company that provides Sodium chloride USP crystal grade active pharmaceutical ingredient (API) or Sodium chloride USP crystal grade finished formulations upon request. The Sodium chloride USP crystal grade suppliers may include Sodium chloride USP crystal grade API manufacturers, exporters, distributors and traders.

click here to find a list of Sodium chloride USP crystal grade suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.

Sodium chloride USP crystal grade USDMF

A Sodium chloride USP crystal grade DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium chloride USP crystal grade active pharmaceutical ingredient (API) in detail. Different forms of Sodium chloride USP crystal grade DMFs exist exist since differing nations have different regulations, such as Sodium chloride USP crystal grade USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Sodium chloride USP crystal grade DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium chloride USP crystal grade USDMF includes data on Sodium chloride USP crystal grade's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium chloride USP crystal grade USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Sodium chloride USP crystal grade suppliers with USDMF on PharmaCompass.

Sodium chloride USP crystal grade JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The Sodium chloride USP crystal grade Drug Master File in Japan (Sodium chloride USP crystal grade JDMF) empowers Sodium chloride USP crystal grade API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the Sodium chloride USP crystal grade JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium chloride USP crystal grade JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of Sodium chloride USP crystal grade suppliers with JDMF on PharmaCompass.

Sodium chloride USP crystal grade KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Sodium chloride USP crystal grade Drug Master File in Korea (Sodium chloride USP crystal grade KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sodium chloride USP crystal grade. The MFDS reviews the Sodium chloride USP crystal grade KDMF as part of the drug registration process and uses the information provided in the Sodium chloride USP crystal grade KDMF to evaluate the safety and efficacy of the drug.

After submitting a Sodium chloride USP crystal grade KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Sodium chloride USP crystal grade API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Sodium chloride USP crystal grade suppliers with KDMF on PharmaCompass.

Sodium chloride USP crystal grade CEP

A Sodium chloride USP crystal grade CEP of the European Pharmacopoeia monograph is often referred to as a Sodium chloride USP crystal grade Certificate of Suitability (COS). The purpose of a Sodium chloride USP crystal grade CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sodium chloride USP crystal grade EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sodium chloride USP crystal grade to their clients by showing that a Sodium chloride USP crystal grade CEP has been issued for it. The manufacturer submits a Sodium chloride USP crystal grade CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sodium chloride USP crystal grade CEP holder for the record. Additionally, the data presented in the Sodium chloride USP crystal grade CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sodium chloride USP crystal grade DMF.

A Sodium chloride USP crystal grade CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sodium chloride USP crystal grade CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Sodium chloride USP crystal grade suppliers with CEP (COS) on PharmaCompass.

Sodium chloride USP crystal grade NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Sodium chloride USP crystal grade as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Sodium chloride USP crystal grade API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Sodium chloride USP crystal grade as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Sodium chloride USP crystal grade and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium chloride USP crystal grade NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Sodium chloride USP crystal grade suppliers with NDC on PharmaCompass.

Sodium chloride USP crystal grade GMP

Sodium chloride USP crystal grade Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Sodium chloride USP crystal grade GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Sodium chloride USP crystal grade GMP manufacturer or Sodium chloride USP crystal grade GMP API supplier for your needs.

Sodium chloride USP crystal grade CoA

A Sodium chloride USP crystal grade CoA (Certificate of Analysis) is a formal document that attests to Sodium chloride USP crystal grade's compliance with Sodium chloride USP crystal grade specifications and serves as a tool for batch-level quality control.

Sodium chloride USP crystal grade CoA mostly includes findings from lab analyses of a specific batch. For each Sodium chloride USP crystal grade CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Sodium chloride USP crystal grade may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium chloride USP crystal grade EP), Sodium chloride USP crystal grade JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium chloride USP crystal grade USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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