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Chemistry

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Also known as: 70458-96-7, Noroxin, Norfloxacine, Chibroxin, Baccidal, Sebercim
Molecular Formula
C16H18FN3O3
Molecular Weight
319.33  g/mol
InChI Key
OGJPXUAPXNRGGI-UHFFFAOYSA-N
FDA UNII
N0F8P22L1P

Norfloxacin
A synthetic fluoroquinolone (FLUOROQUINOLONES) with broad-spectrum antibacterial activity against most gram-negative and gram-positive bacteria. Norfloxacin inhibits bacterial DNA GYRASE.
Norfloxacin is a Quinolone Antimicrobial.
1 2D Structure

Norfloxacin

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
1-ethyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid
2.1.2 InChI
InChI=1S/C16H18FN3O3/c1-2-19-9-11(16(22)23)15(21)10-7-12(17)14(8-13(10)19)20-5-3-18-4-6-20/h7-9,18H,2-6H2,1H3,(H,22,23)
2.1.3 InChI Key
OGJPXUAPXNRGGI-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CCN1C=C(C(=O)C2=CC(=C(C=C21)N3CCNCC3)F)C(=O)O
2.2 Other Identifiers
2.2.1 UNII
N0F8P22L1P
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Am 0715

2. Am 715

3. Am-0715

4. Am-715

5. Am0715

6. Mk 0366

7. Mk 366

8. Mk-0366

9. Mk-366

10. Mk0366

11. Mk366

12. Noroxin

2.3.2 Depositor-Supplied Synonyms

1. 70458-96-7

2. Noroxin

3. Norfloxacine

4. Chibroxin

5. Baccidal

6. Sebercim

7. Mk-366

8. Norfloxacinum

9. Norfloxacino

10. Barazan

11. Fulgram

12. Nflx

13. Am-715

14. 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic Acid

15. 1-ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic Acid

16. Lexinor

17. Zoroxin

18. Mfcd00079532

19. 1,4-dihydro-1-ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic Acid

20. 1-ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-1,4-dihydro-3-quinolinecarboxylic Acid

21. 3-quinolinecarboxylic Acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-

22. Mk-0366

23. Chembl9

24. Chebi:100246

25. 1-ethyl-6-fluor-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-chinolincarbonsaeure

26. 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydroquinoline-3-carboxylic Acid

27. Nsc-757250

28. Mls000069650

29. N0f8p22l1p

30. 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic Acid

31. Ncgc00016916-01

32. Ncgc00016916-09

33. Smr000058200

34. Norfloxacin 100 Microg/ml In Acetonitrile

35. Cas-70458-96-7

36. 3-quinolinecarboxylic Acid, 1,4-dihydro-1-ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-

37. Dsstox_cid_17680

38. Dsstox_rid_79353

39. Dsstox_gsid_37680

40. Norfloxacine [inn-french]

41. Norfloxacinum [inn-latin]

42. Norfloxacino [inn-spanish]

43. Am 715

44. Norphloxacine

45. Norflo

46. Mk 0366

47. Noroxin (tn)

48. Ccris 6302

49. Sr-01000000222

50. Einecs 274-614-4

51. Brn 0567897

52. Unii-n0f8p22l1p

53. Chibroxine

54. Chibroxol

55. Gonorcin

56. Nolicin

57. Noracin

58. Noraxin

59. Norocin

60. Noroxine

61. Norxacin

62. Uroxacin

63. Utinor

64. Noflo

65. Hsdb 8029

66. Norfloxacine,(s)

67. Prestwick_633

68. Norfloxacin [usan:usp:inn:ban:jan]

69. Norfloxacin (norxacin)

70. Norfloxacin - Norxacin

71. Spectrum_001017

72. Norfloxacin [mi]

73. Opera_id_1423

74. Prestwick0_000221

75. Prestwick1_000221

76. Prestwick2_000221

77. Prestwick3_000221

78. Spectrum2_001017

79. Spectrum3_000524

80. Spectrum4_000453

81. Spectrum5_001154

82. Norfloxacin [inn]

83. Norfloxacin [jan]

84. Norfloxacin [usan]

85. Epitope Id:119068

86. Norfloxacin [vandf]

87. Schembl3473

88. Norfloxacin [mart.]

89. Oprea1_375152

90. Bspbio_000261

91. Bspbio_002107

92. Kbiogr_000866

93. Kbioss_001497

94. Norfloxacin [usp-rs]

95. Norfloxacin [who-dd]

96. Mls006011446

97. Bidd:gt0725

98. Divk1c_000084

99. Spectrum1500440

100. Spbio_001173

101. Spbio_002182

102. Bpbio1_000289

103. Zinc3742

104. Norfloxacin (jp17/usp/inn)

105. Dtxsid7037680

106. Bcbcmap01_000218

107. Hms500e06

108. Kbio1_000084

109. Kbio2_001497

110. Kbio2_004065

111. Kbio2_006633

112. Kbio3_001607

113. Norfloxacin [orange Book]

114. Ninds_000084

115. Norfloxacin For System Suitability

116. Hms1568n03

117. Hms1920b16

118. Hms2090f03

119. Hms2091j16

120. Hms2095n03

121. Hms2235g03

122. Hms3712n03

123. Norfloxacin [ep Monograph]

124. Norfloxacin [usp Impurity]

125. Norfloxacin For Peak Identification

126. Pharmakon1600-01500440

127. Act02630

128. Albb-015911

129. Bcp27734

130. Hy-b0132

131. Rkl10074

132. Tox21_110682

133. Tox21_113441

134. 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-quinoline-3-carboxylic Acid

135. 1-ethyl-6-fluoro-4-oxo-7-piperazinylhydroquinoline-3-carboxylic Acid

136. Bbl005569

137. Bdbm50045000

138. Ccg-40235

139. Nsc757250

140. S1509

141. Stk177250

142. Akos000417391

143. Norfloxacin 100 Microg/ml In Ethanol

144. Tox21_110682_1

145. Ac-6855

146. Bcp9000993

147. Cs-1906

148. Db01059

149. Ks-5007

150. Nsc 757250

151. 1-ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-1,4-dihydroquinoline-3-carboxylic Acid

152. Idi1_000084

153. Smp1_000216

154. Ncgc00016916-02

155. Ncgc00016916-03

156. Ncgc00016916-04

157. Ncgc00016916-05

158. Ncgc00016916-06

159. Ncgc00016916-07

160. Ncgc00016916-08

161. Ncgc00016916-11

162. Ncgc00016916-12

163. Ncgc00021725-03

164. Ncgc00021725-04

165. Sy051390

166. Sbi-0051464.p002

167. Ft-0630800

168. Ft-0673085

169. N0817

170. C06687

171. D00210

172. N-8650

173. Ab00052059-18

174. Ab00052059-19

175. Ab00052059_20

176. Ab00052059_21

177. Norfloxacin, Analytical Standard, >=98% (tlc)

178. Norfloxacin, Vetranal(tm), Analytical Standard

179. 458n967

180. Norfloxacin, Antibiotic For Culture Media Use Only

181. Q417897

182. Sr-01000000222-2

183. Sr-01000000222-3

184. Brd-k11196887-001-05-5

185. Brd-k11196887-001-15-4

186. Z56926638

187. Norfloxacin, British Pharmacopoeia (bp) Reference Standard

188. Norfloxacin, European Pharmacopoeia (ep) Reference Standard

189. 1-ethyl-3-carboxy-6-fluoro-7-(piperazinyl-1)-quinolin-4(1h)-one

190. Norfloxacin, United States Pharmacopeia (usp) Reference Standard

191. Norfloxacin, Pharmaceutical Secondary Standard; Certified Reference Material

192. (nflx)1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-quinoline-3-carboxylic Acid

193. 1-ethyl-1,4-dihydro-6-fluoro-4-oxo-7-(1-piperazinyl)quinoline-3-carboxylic Acid

194. 1-ethyl-4-oxo-6-fluoro-7-(piperazinyl)-1,4-dihydro-quinoline-3-carboxylic Acid

195. 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline Carboxylic Acid

196. 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-quinoline-3-carboxylicacid

197. 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)quinoline-3-carboxylic Acid

198. 1-ethyl-6-fluoro-1,4-dihydro-7-(1-piperazinyl)-4-oxo-3-quinoline Carboxylic Acid

199. 1-ethyl-6-fluoro-1,4-dihydro-7-(1-piperazinyl)-4-oxoquinoline-3-carboxylic Acid

200. 1-ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-1,4-dihydro-3-quinolinecarboxylic Acid #

201. 1-ethyl-6-fluoro-7-(1-piperazinyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic Acid

202. 1-ethyl-6-fluoro-7-(1-piperazinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid

203. 7-(1-piperazinyl)-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid

204. Norfloxacin For Peak Identification, European Pharmacopoeia (ep) Reference Standard

205. Norfloxacin For System Suitability, European Pharmacopoeia (ep) Reference Standard

206. (norfloxacin)1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-quinoline-3-carboxylic Acid

207. 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,4,4a,8a-tetrahydro-quinoline-3-carboxylic Acid (norfloxacin)

208. 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-quinoline-3-carboxylic Acid (norfloxacin)

209. 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-quinoline-3-carboxylic Acid(1-norfloxacin)

210. 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-quinoline-3-carboxylic Acid(norfloxacin)

2.4 Create Date
2005-03-25
3 Chemical and Physical Properties
Molecular Weight 319.33 g/mol
Molecular Formula C16H18FN3O3
XLogP3-1
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count3
Exact Mass319.13321961 g/mol
Monoisotopic Mass319.13321961 g/mol
Topological Polar Surface Area72.9 Ų
Heavy Atom Count23
Formal Charge0
Complexity519
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Drug and Medication Information
4.1 Therapeutic Uses

Anti-Bacterial Agents; Enzyme Inhibitors; Nucleic Acid Synthesis Inhibitors

National Library of Medicine's Medical Subject Headings online file (MeSH, 2012)


Oral norfloxacin is used for the treatment of prostatitis caused by E. coli. /Included in US product label/

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 397


Oral norfloxacin is used in adults for the treatment of complicated UTIs caused by susceptible E. coli, K. pneumoniae, P. mirabilis, Ps. aeruginosa, S. marcescens, or E. faecalis. /Included in US product label/

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 397


Oral norfloxacin is used in adults for the treatment of uncomplicated urinary tract infections (UTIs) (including cystitis) caused by susceptible Citrobacter freundii, Enterobacter aerogenes, E. cloacae, Escherichia coli, Klebsiella pneumoniae, ... Proteus mirabilis, P. vulgaris, ... Pseudomonas aeruginosa, ... . The drug also is used orally in adults for the treatment of uncomplicated UTIs caused by susceptible Staphylococcus aureus, S. epidermidis, S. saprophyticus, Streptococcus agalactiae (group B streptococci), or Enterococcus faecalis. /Included in US product label/

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 397


For more Therapeutic Uses (Complete) data for Norfloxacin (10 total), please visit the HSDB record page.


4.2 Drug Warning

WARNING: Fluoroquinolones, including Noroxin, are associated with an increased risk of tendinitis and tendon rupture in all ages. This risk is further increased in older patients usually over 60 years of age, in patients taking corticosteroid drugs, and in patients with kidney, heart or lung transplants.

US Natl Inst Health; DailyMed. Current Medication Information for NOROXIN (Norfloxacin) tablet, film coated (February 2012). Available from, as of March 2, 2012: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=36087c76-5da9-4fab-e88f-da1d5a579d8e


WARNING: Fluoroquinolones, including Noroxin, may exacerbate muscle weakness in persons with myasthenia gravis. Avoid Noroxin in patients with known history of myasthenia gravis

US Natl Inst Health; DailyMed. Current Medication Information for NOROXIN (Norfloxacin) tablet, film coated (February 2012). Available from, as of March 2, 2012: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=36087c76-5da9-4fab-e88f-da1d5a579d8e


Serious and occasionally fatal hypersensitivity (anaphylactic) reactions, some following the first dose, have been reported in patients receiving quinolone therapy, including Noroxin. Some reactions were accompanied by cardiovascular collapse, loss of consciousness, tingling, pharyngeal or facial edema, dyspnea, urticaria and itching. Only a few patients had a history of hypersensitivity reactions. If an allergic reaction to norfloxacin occurs, discontinue the drug. Serious acute hypersensitivity reactions require immediate emergency treatment with epinephrine. Oxygen, intravenous fluids, antihistamines, corticosteroids, pressor amines, and airway management, including intubation, should be administered as indicated.

US Natl Inst Health; DailyMed. Current Medication Information for NOROXIN (Norfloxacin) tablet, film coated (February 2012). Available from, as of March 2, 2012: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=36087c76-5da9-4fab-e88f-da1d5a579d8e


Other serious and sometimes fatal events, some due to hypersensitivity, and some due to uncertain etiology, have been reported rarely in patients receiving therapy with quinolones, including Noroxin. These events may be severe and generally occur following the administration of multiple doses. Clinical manifestations may include one or more of the following: fever, rash or severe dermatologic reactions (e.g., toxic epidermal necrolysis, Stevens-Johnson syndrome); vasculitis; arthralgia; myalgia; serum sickness; allergic pneumonitis; interstitial nephritis; acute renal insufficiency or failure; hepatitis; jaundice; acute hepatic necrosis or failure; anemia, including hemolytic and aplastic; thrombocytopenia, including thrombotic thrombocytopenic purpura; leukopenia; agranulocytosis; pancytopenia; and/or other hematologic abnormalities.

US Natl Inst Health; DailyMed. Current Medication Information for NOROXIN (Norfloxacin) tablet, film coated (February 2012). Available from, as of March 2, 2012: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=36087c76-5da9-4fab-e88f-da1d5a579d8e


For more Drug Warnings (Complete) data for Norfloxacin (24 total), please visit the HSDB record page.


4.3 Drug Indication

For the treatment of urinary tract infection


FDA Label


5 Pharmacology and Biochemistry
5.1 Pharmacology

Norfloxacin is a quinolone/fluoroquinolone antibiotic. Norfloxacin is bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase, which allows the untwisting required to replicate one DNA double helix into two. Notably the drug has 100 times higher affinity for bacterial DNA gyrase than for mammalian.


5.2 MeSH Pharmacological Classification

Cytochrome P-450 CYP1A2 Inhibitors

Drugs and compounds which inhibit or antagonize the biosynthesis or actions of CYTOCHROME P-450 CYP1A2. (See all compounds classified as Cytochrome P-450 CYP1A2 Inhibitors.)


Anti-Bacterial Agents

Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)


Topoisomerase II Inhibitors

Compounds that inhibit the activity of DNA TOPOISOMERASE II. Included in this category are a variety of ANTINEOPLASTIC AGENTS which target the eukaryotic form of topoisomerase II and ANTIBACTERIAL AGENTS which target the prokaryotic form of topoisomerase II. (See all compounds classified as Topoisomerase II Inhibitors.)


5.3 FDA Pharmacological Classification
5.3.1 Active Moiety
NORFLOXACIN
5.3.2 FDA UNII
N0F8P22L1P
5.3.3 Pharmacological Classes
Chemical Structure [CS] - Quinolones
5.4 ATC Code

J01MA06

S76 | LUXPHARMA | Pharmaceuticals Marketed in Luxembourg | Pharmaceuticals marketed in Luxembourg, as published by d'Gesondheetskeess (CNS, la caisse nationale de sante, www.cns.lu), mapped by name to structures using CompTox by R. Singh et al. (in prep.). List downloaded from https://cns.public.lu/en/legislations/textes-coordonnes/liste-med-comm.html. Dataset DOI:10.5281/zenodo.4587355


J - Antiinfectives for systemic use

J01 - Antibacterials for systemic use

J01M - Quinolone antibacterials

J01MA - Fluoroquinolones

J01MA06 - Norfloxacin


S - Sensory organs

S01 - Ophthalmologicals

S01A - Antiinfectives

S01AE - Fluoroquinolones

S01AE02 - Norfloxacin


5.5 Absorption, Distribution and Excretion

Absorption

Rapid


Route of Elimination

Norfloxacin is eliminated through metabolism, biliary excretion, and renal excretion. It is expected to undergo both glomerular filtration and tubular secretion during renal excretion, as shown by its high renal clearance rate of approximately 275 mL/min.


Norfloxacin crosses the placenta and is distributed into cord blood and amniotic fluid. It is not known whether the drug is distributed into milk. Norfloxacin was not detected in the milk of lactating women following a single 200-mg oral dose of the drug, but the possibility of distribution into milk following higher doses remains to be determined. Some other quinolones (e.g., ciprofloxacin, levofloxacin ofloxacin) are distributed into milk.

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 404


In adults who received 400 mg of oral norfloxacin twice daily, prostatic tissue concentrations of the drug ranged from 0.24-4.65 ug/g in specimens obtained 1-4 hours after the second dose; concurrent serum concentrations ranged from 0.42-5.3 ug/mL. Norfloxacin is 10-15% bound to serum proteins.

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 404


Biliary concentrations of norfloxacin may be up to 10 times higher than concurrent serum concentrations. In cholecystectomy patients who received a single 400-mg oral dose of norfloxacin prior to surgery, concentrations of the drug ranged from 0.6-15.6 ug/mL in gallbladder bile, from 0.4-7.5 mcg/g in gallbladder tissue, and from 0.4-1.8 ug/mL in serum in specimens obtained approximately 3.5-6 hours after the dose.

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 404


There is limited information on the distribution of norfloxacin. Following oral administration in adults, norfloxacin is distributed into renal parenchyma, gallbladder, liver, prostatic tissue, testicles, seminal fluid, uterus, fallopian tubes, cervical and vaginal tissue, blister fluid, tonsils, maxillary sinus mucosa, sputum, and bile.

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 404


For more Absorption, Distribution and Excretion (Complete) data for Norfloxacin (9 total), please visit the HSDB record page.


5.6 Metabolism/Metabolites

Via liver and kidney


Norfloxacin is eliminated by renal and nonrenal mechanisms. The drug is partially metabolized by modification of the piperazinyl group to 6 metabolites, designated M-1, M-2, M-3, M-4(1), M-4(2), and M-5.2 Although some of the metabolites are microbiologically active, they are less active than the parent drug. It has been suggested that norfloxacin undergoes first-pass metabolism in the liver, but further study is needed to fully elucidate the metabolic fate of the drug.

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 404


Pefloxacin, N-desmethyl is a known human metabolite of Pefloxacin.

S73 | METXBIODB | Metabolite Reaction Database from BioTransformer | DOI:10.5281/zenodo.4056560


5.7 Biological Half-Life

3-4 hours


In patients with impaired renal function, serum concentrations of norfloxacin are higher and its half-life is prolonged. In adults with renal impairment, the half-life of norfloxacin averaged 4.4, 6.6, or 7.6 hours in adults with creatinine clearances of 30-80, 10-29, or less than 10 mL/minute per 1.73 sq m, respectively. Limited data suggest that half-life of the drug is not substantially affected by hepatic impairment.

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 404


The effective plasma or serum half-life of norfloxacin in adults with normal renal function is 2.3-4 hours. The effective half-life of the drug averages 4 hours in geriatric individuals 65-75 years of age with renal function normal for their age.

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 404


5.8 Mechanism of Action

The bactericidal action of Norfloxacin results from inhibition of the enzymes topoisomerase II (DNA gyrase) and topoisomerase IV, which are required for bacterial DNA replication, transcription, repair, and recombination. Norfloxacin is a broad-spectrum antibiotic agent that is shown to be effective against various Gram-positive and Gram-negative bacterial species. The fluorine atom at the 6 position increases potency against gram-negative organisms, and the piperazine moiety at the 7 position is responsible for anti-pseudomonal activity


Norfloxacin usually is bactericidal in action. Like other fluoroquinolone anti-infectives, norfloxacin inhibits DNA synthesis in susceptible organisms via inhibition of type II DNA topoisomerases (DNA gyrase, topoisomerase IV).

American Society of Health-System Pharmacists 2011; Drug Information 2011. Bethesda, MD. 2011, p. 401


Fluoroquinolones prolong the QT interval by blocking voltage-gated potassium channels, especially the rapid component of the delayed rectifier potassium current I(Kr), expressed by HERG (the human ether-a-go-go-related gene). According to the available case reports and clinical studies, moxifloxacin carries the greatest risk of QT prolongation from all available quinolones in clinical practice and it should be used with caution in patients with predisposing factors for Torsades de pointes (TdP).

PMID:22156660 Briasoulis A et al; Cardiology 120 (2): 103-10 (2011)


API Reference Price

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CHINA","customerAddress":"MEDREICH HOUSE, NO12\/8,"},{"dataSource":"API Import","activeIngredients":"","year":"2024","qtr":"Q3","strtotime":1720031400,"product":"NORFLOXACIN USP","address":"CADILA CORPORATE CAMPUS","city":"AHMEDABAD, GUJARAT","supplier":"HENAN KANGTAI PHARMACEUTICAL CO., LTD.","supplierCountry":"CHINA","foreign_port":"BEIJING","customer":"CADILA PHARMACEUTICALS","customerCountry":"INDIA","quantity":"50.00","actualQuantity":"50","unit":"KGS","unitRateFc":"38","totalValueFC":"1928.8","currency":"USD","unitRateINR":"3203.4","date":"04-Jul-2024","totalValueINR":"160170","totalValueInUsd":"1928.8","indian_port":"Ahmedabad Air","hs_no":"29419060","bill_no":"4317641","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"BEIJING","supplierAddress":"NO.338 KANGTAI ROAD, SISHUI TOWN, XINGYANG ZHENGZHOU CHINA, , ChinaSDNF China","customerAddress":"CADILA CORPORATE CAMPUS"}]
01-Jan-2021
24-Aug-2024
KGS
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Average Price (USD/KGS)

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Total Value (USD)

Quantity (KGS) & Unit rate (USD/KGS) over time

API Imports and Exports

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