Synopsis
Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Australia
DRUG PRODUCT COMPOSITIONS
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
1. Sulfate, Zinc
2. Zinc Sulfate, Heptahydrate
3. Zincteral
1. Zinc Sulphate
2. 7733-02-0
3. Zinc Sulfate Anhydrous
4. Zincate
5. Zinc Sulfate (1:1)
6. Znso4
7. Sulfuric Acid, Zinc Salt (1:1)
8. Sulfate De Zinc
9. Zinc(ii) Sulfate
10. Zinc Sulphate Anhydrous
11. Zinc Sulfate, Anhydrous
12. Zinc Sulphate, Anhydrous
13. Zinc Sulfate (anhydrous)
14. Zinc Sulfate Hydrate
15. 0j6z13x3wo
16. Chebi:35176
17. Nsc-32677
18. Nsc-135806
19. Complexonat
20. Medizinc
21. Optised
22. Orazinc
23. Solvezinc
24. Zinklet
25. Neozin
26. Visine-ac
27. Zinci Sulfas
28. Prefrin-z
29. Zincum Sulfuricum
30. Zink-gro
31. Zinc Sulfate Solution
32. Zinc Vitriol (van)
33. Caswell No. 927
34. White Vitriol (van)
35. Zincsulphate
36. Salvazinc
37. Zinc;sulfate
38. Nu-z
39. Sulfuric Acid, Zinc Salt
40. Zinc-200
41. Sulfate De Zinc [french]
42. Ccris 3664
43. Sulfuric Acid Zinc Salt (van)
44. Hsdb 1063
45. Einecs 231-793-3
46. Nsc 32677
47. Epa Pesticide Chemical Code 089001
48. Nsc 135806
49. Unii-0j6z13x3wo
50. Ai3-03967
51. Sulfato De Cinc
52. Zinc(ii)sulfate
53. Sulfato De Zinco
54. Solfato Di Zinco
55. Zinc (as Sulfate)
56. Zinc(2+) Sulfate
57. Mfcd00011302
58. Zinc (as Sulphate)
59. Zinc Sulphate Hydrate
60. Zinci Sulfas Monohydrate
61. Zinc Suflate Monohydrate
62. Zinc Sulfate, Unspecified
63. Zinc Sulfate [mi]
64. Zinc Sulphate Nanoparticles
65. Ec 231-793-3
66. Zinc Sulfate [hsdb]
67. Zinc Sulfate, Unspecified Form
68. Chembl1200929
69. Dtxsid2040315
70. Akos025295737
71. Zinc Sulfate, 100mm Aqueous Solution
72. Db09322
73. Q204954
74. J-010404
Molecular Weight | 161.4 g/mol |
---|---|
Molecular Formula | O4SZn |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 0 |
Exact Mass | 159.880871 g/mol |
Monoisotopic Mass | 159.880871 g/mol |
Topological Polar Surface Area | 88.6 Ų |
Heavy Atom Count | 6 |
Formal Charge | 0 |
Complexity | 62.2 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
Mesh Heading: Astringent
National Library of Medicine, SIS; ChemIDplus Record for Zinc Sulfate. (7733-02-0). Available from, as of April 17, 2006: https://chem.sis.nlm.nih.gov/chemidplus/chemidlite.jsp
Dietary supplement ingredient in use before October 15, 1994 (Mineral and trace element) /Date of the Dietary Supplement Health and Education Act of 1994/..
NNFA List of Dietary Supplement Ingredients In Use Before October 15, 1994. Available from, as of December 8, 2006: https://www.fda.gov/ohrms/dockets/dockets/05p0305/05p-0305-cr00001-03-NNFA-List-vol1.pdf
MEDICATION (VET): Zinc sulfate, USP, applied topically in 10% aqueous solution, is highly effective in treatment of foot rot in sheep.
Booth, N.H., L.E. McDonald (eds.). Veterinary Pharmacology and Therapeutics. 5th ed. Ames, Iowa: Iowa State University Press, 1982., p. 670
MEDICATION (VET): Useful antiseptic astringent for ophthalmic use as aqueous solution or ointment (0.25-0.5%). Spraying sheep with 0.25% solution after shearing reduced incidence of infected wounds. 1% solutions have been used on granular vaginitis lesions of cows, posthitis of rams, and make excellent detergent, odorless, antiseptic egg wash. ... As white lotion ... on bruised, inflamed, pruritic skin areas on cows and horses.
Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 669
For more Therapeutic Uses (Complete) data for ZINC SULFATE (26 total), please visit the HSDB record page.
... Zinc sulfate often is an effective /emetic/, but potential hemolytic and renal toxicity is too great to recommend use ... .
American Medical Association, AMA Department of Drugs. AMA Drug Evaluations. 5th ed. Chicago: American Medical Association, 1983., p. 489
Thiazide diuretics have been found to increase urinary zinc excretion. /Zinc supplements/
Thomson/Micromedex. Drug Information for the Health Care Professional. Volume 1, Greenwood Village, CO. 2006.
Large doses of zinc may inhibit copper absorption in the intestine; zinc supplements should be taken at least 2 hours after the administration of copper supplements. /Zinc supplements/
Thomson/Micromedex. Drug Information for the Health Care Professional. Volume 1, Greenwood Village, CO. 2006.
Patients using zinc sulfate ophthalmic solutions should be advised to discontinue the drug and consult a physician if ocular pain or visual changes occur, they experience continued ocular redness or irritation, or the condition worsens or persists for more than 3 days.
McEvoy, G.K. (ed.). American Hospital Formulary Service. AHFS Drug Information. American Society of Health-System Pharmacists, Bethesda, MD. 2006., p. 2761
For more Drug Warnings (Complete) data for ZINC SULFATE (15 total), please visit the HSDB record page.
This medication is a mineral used to treat or prevent low levels of zinc alone and together with oral rehydration therapy (ORT). It is also used as a topical astringent. Zinc Sulfate Injection, USP is indicated for use as a supplement to intravenous solutions given for TPN.
Zinc sulfate is a common zinc supplement in parenteral nutrition.
Zinc has been identified as a cofactor for over 70 different enzymes, including alkaline phosphatase, lactic dehydrogenase and both RNA and DNA polymerase. Zinc facilitates wound healing, helps maintain normal growth rates, normal skin hydration and the senses of taste and smell.
Astringents
Agents, usually topical, that cause the contraction of tissues for the control of bleeding or secretions. (See all compounds classified as Astringents.)
A - Alimentary tract and metabolism
A12 - Mineral supplements
A12C - Other mineral supplements
A12CB - Zinc
A12CB01 - Zinc sulfate
B - Blood and blood forming organs
B05 - Blood substitutes and perfusion solutions
B05X - I.v. solution additives
B05XA - Electrolyte solutions
B05XA18 - Zinc sulfate
Absorption
Approximately 20 to 30% of dietary zinc is absorbed, primarily from the duodenum and ileum. The amount absorbed is dependent on the bioavailability from food. Zinc is the most bioavailable from red meat and oysters. Phytates may impair absorption by chelation and formation of insoluble complexes at an alkaline pH. After absorption, zinc is bound in the intestine to the protein metallothionein. Endogenous zinc can be reabsorbed in the ileum and colon, creating an enteropancreatic circulation of zinc.
Route of Elimination
Primarily fecal (approximately 90%); to a lesser extent in the urine and in perspiration.
Volume of Distribution
After absorption zinc is bound to protein metallothionein in the intestines. Zinc is widely distributed throughout the body. It is primarily stored in RBCs, WBCs, muscles, bones, Skin, Kidneys, Liver, Pancreas, retina, and prostate.
The pharmacokinetics of zinc sulfate were compared with those of a new zinc pantothenate, in rabbits. Each salt was administered to rabbits at a dosage of 3.3 uCi of zinc-65/kg of body weight. The measured pharmacokinetics of the two compounds responded to a two compartment open model. The urinary elimination of the two salts was similar, as was their localization in the skin and fur, but Zn pantothenate was retained by the liver to a lesser extent than was zinc sulfate (ZnSO4).
PMID:6520772 Guillard O et al; J Pharm Sci 73 (11): 1642-3 (1984)
Absorption: 20% to 30%. Protein binding: 99%. Elimination: Through small bowel excretion.
Lelkin, J.B., Paloucek, F.P., Poisoning & Toxicology Compendium. LEXI-COMP Inc. & American Pharmaceutical Association, Hudson, OH 1998., p. 573
In women in different trimesters of pregnancy, the oral administration of 200 mg zinc sulfate per day resulted in an increase of serum zinc levels from 109.7 to 205.4 mg/dL. In the control group, serum zinc levels declined from 113.0 mg/dL in the first trimester to 83.8 in the third trimester.
Bingham, E.; Cohrssen, B.; Powell, C.H.; Patty's Toxicology Volumes 1-9 5th ed. John Wiley & Sons. New York, N.Y. (2001)., p. 2:267
...An absorption half-life of 0.4 hr /was reported/ when 45 mg Zn2+ as zinc sulfate was administered once in gelatine capsules to 10 healthy young men. Serum concentrations were measured frequently during a total investigation time of 8 hours. A mean maximum concentration of 8.2 umol Zn2+/L serum was found after 2.3 hours (tmax). There is evidence of an enteral recirculation, the first rebound effect appeared after 1.4 hours during the absorption phase before tmax was reached, and exhibited mean reabsorption rates of 70% of the dose given. The subsequent ones (max. of 5) appeared at regular intervals of 1.2 hours with a decrease of the quantity reabsorbed.
European Chemicals Bureau; EU Risk Assessment Report- Zinc sulphate, Vol.46 p.31 (2004). Available from, as of June 29, 2006: https://esis.jrc.ec.europa.eu/
For more Absorption, Distribution and Excretion (Complete) data for ZINC SULFATE (14 total), please visit the HSDB record page.
3 hours
Half-life: 3 hours
Lelkin, J.B., Paloucek, F.P., Poisoning & Toxicology Compendium. LEXI-COMP Inc. & American Pharmaceutical Association, Hudson, OH 1998., p. 573
Zinc inhibits cAMP-induced, chloride-dependent fluid secretion by inhibiting basolateral potassium (K) channels, in in-vitro studies with rat ileum. This study has also shown the specificity of Zn to cAMP-activated K channels, because zinc did not block the calcium (Ca)-mediated K channels. As this study was not performed in Zn-deficient animals, it provides evidence that Zn is probably effective in the absence of Zn deficiency. Zinc also improves the absorption of water and electrolytes, improves regeneration of the intestinal epithelium, increases the levels of brush border enzymes, and enhances the immune response, allowing for a better clearance of the pathogens.
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
---|
Upgrade, download data, analyse, strategize, subscribe with us
Details:
Undisclosed
Lead Product(s): Zinc Sulphate,Inapplicable
Therapeutic Area: Genetic Disease Brand Name: Undisclosed
Study Phase: Phase II/ Phase IIIProduct Type: Other Small Molecule
Sponsor: Global Health Uganda | Makerere University
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 19, 2024
Lead Product(s) : Zinc Sulphate,Inapplicable
Therapeutic Area : Genetic Disease
Highest Development Status : Phase II/ Phase III
Partner/Sponsor/Collaborator : Global Health Uganda | Makerere University
Deal Size : Inapplicable
Deal Type : Inapplicable
Zinc for Infection Prevention in Sickle Cell Anemia-2 (ZIPS-2)
Details : Undisclosed
Product Name : Undisclosed
Product Type : Other Small Molecule
Upfront Cash : Inapplicable
August 19, 2024
Details:
Zinc Sulfate is a trace element indicated as a source of zinc for parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated.
Lead Product(s): Zinc Sulphate,Inapplicable
Therapeutic Area: Neurology Brand Name: Zinc Sulfate-Generic
Study Phase: Approved FDFProduct Type: Other Small Molecule
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 18, 2022
Lead Product(s) : Zinc Sulphate,Inapplicable
Therapeutic Area : Neurology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Piramal Critical Care Launches First to Market Generic Zinc Sulfate Injection in the U.S.
Details : Zinc Sulfate is a trace element indicated as a source of zinc for parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated.
Product Name : Zinc Sulfate-Generic
Product Type : Other Small Molecule
Upfront Cash : Inapplicable
August 18, 2022
Details:
Undisclosed
Lead Product(s): Lactobacillus reuteri DSM17938,Zinc Sulphate
Therapeutic Area: Infections and Infectious Diseases Brand Name: Undisclosed
Study Phase: Phase II/ Phase IIIProduct Type: Probiotic
Sponsor: BioGaia Pharma
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable November 29, 2012
Lead Product(s) : Lactobacillus reuteri DSM17938,Zinc Sulphate
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Phase II/ Phase III
Partner/Sponsor/Collaborator : BioGaia Pharma
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Undisclosed
Product Name : Undisclosed
Product Type : Probiotic
Upfront Cash : Inapplicable
November 29, 2012
Details:
Undisclosed
Lead Product(s): Zinc Sulphate,Inapplicable
Therapeutic Area: Infections and Infectious Diseases Brand Name: Undisclosed
Study Phase: UndisclosedProduct Type: Other Small Molecule
Sponsor: World Health Organization
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable October 28, 2010
Lead Product(s) : Zinc Sulphate,Inapplicable
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Undisclosed
Partner/Sponsor/Collaborator : World Health Organization
Deal Size : Inapplicable
Deal Type : Inapplicable
Effect of Zinc Supplementation on Response to Oral Polio Vaccine in Infants in Pakistan
Details : Undisclosed
Product Name : Undisclosed
Product Type : Other Small Molecule
Upfront Cash : Inapplicable
October 28, 2010
RLD : No
TE Code :
Brand Name : ZINC SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG ZINC/ML
Approval Date : 1987-05-05
Application Number : 19229
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Approval Date : 2019-07-18
Application Number : 209377
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Approval Date : 2020-04-15
Application Number : 209377
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : No
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Approval Date : 2025-05-01
Application Number : 219585
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Approval Date : 2022-12-27
Application Number : 216145
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Approval Date : 2022-05-03
Application Number : 216249
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Approval Date : 2022-05-03
Application Number : 216249
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Approval Date : 2024-07-05
Application Number : 214597
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Approval Date : 2024-07-05
Application Number : 214597
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Approval Date : 2025-06-10
Application Number : 217624
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Italy
Brand Name : Zinc Imizol
Dosage Form :
Dosage Strength : Coll 10 Ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Generic
Registration Country : Turkey
Ferrous Fumarate; Zinc Sulfate; Copper Sulfate; Magnesium Sulfate; Ascorbic Acid; Pyridoxine; Vitamin B 12; Folic Acid
Brand Name : Eurofar
Dosage Form : CAPSULE
Dosage Strength :
Packaging : 30 Tablets
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : Generic
Registration Country : Turkey
Brand Name : Zinconet C
Dosage Form : SYRUP
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info :
Registration Country : Sweden
Brand Name : Solvezink
Dosage Form : EFFERVESCENT TABLET
Dosage Strength : 45 MG ZN 2+
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Italy
Brand Name : Zinc Sulphate
Dosage Form :
Dosage Strength : 30 Cpr 200 Mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Norway
Brand Name : Solvezink
Dosage Form : Tablet
Dosage Strength : 45 mg Zn
Packaging : Box
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Related Excipient Companies
Excipients by Applications
Dosage Form : Orodispersible Tablet, Tablet
Grade : Oral
Category : Chewable & Orodispersible Aids, Direct Compression, Fillers, Diluents & Binders, Taste Masking
Application : Chewable & Orodispersible Aids, Direct Compression, Fillers, Diluents & Binders, Taste Masking
Excipient Details : CS90 is a directly compressible calcium carbonate with starch used for chewable tablets due to its smooth mouthfeel and creamy texture.
Pharmacopoeia Ref : NA
Technical Specs : PSD D50: 150-175 µm, Tapped Density: 0.85
Ingredient(s) : Calcium Carbonate Excipient
Dosage Form : Capsule, Granule / Pellet, Tablet, Injectable / Parenteral
Grade : Parenteral, Oral
Category : Fillers, Diluents & Binders, Thickeners and Stabilizers
Dosage Form : Capsule, Granule / Pellet, Tablet, Injectable / Parenteral
Grade : Parenteral, Oral
Category : Fillers, Diluents & Binders, Thickeners and Stabilizers
Dosage Form : Capsule, Granule / Pellet, Tablet, Injectable / Parenteral
Grade : Parenteral, Oral
Category : Fillers, Diluents & Binders, Thickeners and Stabilizers
Grade : Oral
Category : Co-Processed Excipients, Fillers, Diluents & Binders
Application : Co-Processed Excipients, Fillers, Diluents & Binders
Excipient Details : ProBlend (SMCC) is a co-processed excipient consists of microcrystalline cellulose & colloidal silicon dioxide, used as a diluent & binder in OSDs.
Pharmacopoeia Ref : USP-NF, DMF, EXCiPAT, KOSHER, ...
Technical Specs : NA
Ingredient(s) : Silicified Microcrystalline Cellulose
Dosage Form : Capsule, Granule / Pellet, Tablet, Injectable / Parenteral
Grade : Parenteral, Oral
Category : Fillers, Diluents & Binders, Thickeners and Stabilizers
Dosage Form : Tablet
Grade : Oral
Category : Direct Compression, Fillers, Diluents & Binders, Taste Masking
Application : Direct Compression, Fillers, Diluents & Binders, Taste Masking
Excipient Details : CM90 is a directly compressible, granulated calcium carbonate with maltodextrin used for swallow tablets due to its high density and compressibility.
Pharmacopoeia Ref : NA
Technical Specs : PSD D50: 490- 500 µm; Tapped Density: 1.50
Ingredient(s) : Calcium Carbonate Excipient
Grade : Oral
Category : Fillers, Diluents & Binders, Lubricants & Glidants
Application : Fillers, Diluents & Binders, Lubricants & Glidants
Excipient Details : Most popular excipient for the production of tablets and capsules. Offering an efficient and low dosage in capsules.
Pharmacopoeia Ref : Monograph- Ph.Eur, USP/NF
Technical Specs : Specific Surface Area-6-10 m2/g; Particle Size-7-11 µm
Ingredient(s) : Magnesium Stearate
Application : Lubricants & Glidants
Excipient Details : TABLUBE is one of the oldest and most widely used lubricants for tablet, capsules and other solid dosage forms.
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Magnesium Stearate
Brand Name : Magnesium Stearate
Application : Lubricants & Glidants
Excipient Details : Magnesium stearate is the magnesium salt of stearic acid. It acts as a lubricating agent in tablet manufacturing.
Pharmacopoeia Ref : USP/BP/EP/PH.EUR
Technical Specs : Not Available
Ingredient(s) : Magnesium Stearate
Grade : Oral
Category : Fillers, Diluents & Binders, Lubricants & Glidants
Application : Fillers, Diluents & Binders, Lubricants & Glidants
Excipient Details : Higher specific surface area and a smaller median particle size. This product is preferred for more critical and very fine herbal formulations.
Pharmacopoeia Ref : Monograph- Ph.Eur, USP/NF
Technical Specs : Specific Surface Area-8-12 m2/g; Particle Size-5-9 µm
Ingredient(s) : Magnesium Stearate
Brand Name : Magnesium Stearate
Application : Lubricants & Glidants
Excipient Details : Lubricants, Anti-adhesive, Glidant
Grade : Oral
Category : Fillers, Diluents & Binders, Lubricants & Glidants
Application : Fillers, Diluents & Binders, Lubricants & Glidants
Pharmacopoeia Ref : Monograph- Ph.Eur, USP/NF
Technical Specs : Specific Surface Area-6-8 m2/g; Particle Size-7-11 µm
Ingredient(s) : Magnesium Stearate
Application : Emulsifying Agents, Lubricants & Glidants
Excipient Details : Glidant; Emulsion Stabilizer; Anti-caking Agent.
Grade : Oral
Category : Fillers, Diluents & Binders, Lubricants & Glidants
Application : Fillers, Diluents & Binders, Lubricants & Glidants
Pharmacopoeia Ref : Monograph- Ph.Eur, USP/NF
Technical Specs : Not Available
Ingredient(s) : Magnesium Stearate
Dosage Form : Tablet
Grade : Oral
Category : Chewable & Orodispersible Aids, Co-Processed Excipients, Direct Compression, Taste Masking
Grade : Oral
Category : Co-Processed Excipients, Fillers, Diluents & Binders
Application : Co-Processed Excipients, Fillers, Diluents & Binders
Excipient Details : ProBlend (SMCC) is a co-processed excipient consists of microcrystalline cellulose & colloidal silicon dioxide, used as a diluent & binder in OSDs.
Pharmacopoeia Ref : USP-NF, DMF, EXCiPAT, KOSHER, ...
Technical Specs : NA
Ingredient(s) : Silicified Microcrystalline Cellulose
Application : Co-Processed Excipients, Fillers, Diluents & Binders
Excipient Details : Microlose (Lactose Monohydrate & Microcrystalline Cellulose) is used as a diluent in oral dosage forms such as tablets.
Pharmacopoeia Ref : DMF, EXCiPAT, KOSHER, HALAL, W...
Technical Specs : Lactose Monohydrate – 40%, Microcrystalline cellulose – 60%
Ingredient(s) : Lactose Monohydrate
Dosage Form : Tablet, Orodispersible Tablet
Grade : Oral
Category : Chewable & Orodispersible Aids, Co-Processed Excipients, Taste Masking
Application : Chewable & Orodispersible Aids, Co-Processed Excipients, Taste Masking
Excipient Details : HiCel CE15 offers a superior mouthfeel with less chalkiness and gritness in chewable tablets and orally disintegrating tablets (ODTs).
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Guar Gum Excipient
Brand Name : HiCel MCC Spheres
Application : Co-Processed Excipients, Controlled & Modified Release
Excipient Details : HiCel MCC Spheres are extremely versatile which are used for controlled release or sustained release formulations.
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose
Dosage Form : Tablet
Grade : Oral
Category : Co-Processed Excipients, Direct Compression, Fillers, Diluents & Binders, Lubricants & Glidants
Application : Co-Processed Excipients, Direct Compression, Fillers, Diluents & Binders, Lubricants & Glidants
Excipient Details : HiCel SMCC has unique combination which result in optimum compaction & superior flow properties.
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose
Dosage Form : Tablet, Emulsion, Suspension
Grade : Oral
Category : Co-Processed Excipients, Fillers, Diluents & Binders, Rheology Modifiers
Application : Co-Processed Excipients, Fillers, Diluents & Binders, Rheology Modifiers
Excipient Details : HiCel MCG is use in oral suspensions as a stabilizer. It is a good binder for tablets & excellent thickener as well.
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Carboxymethyl cellulose sodium
Dosage Form : Tablet
Grade : Oral
Category : Co-Processed Excipients, Direct Compression, Disintegrants & Superdisintegrants
Dosage Form : Capsule, Tablet, Dry Syrup
Grade : Oral
Category : Co-Processed Excipients, Direct Compression, Solubilizers
Application : Co-Processed Excipients, Direct Compression, Solubilizers
Excipient Details : Solubilizer
Pharmacopoeia Ref : Not Available
Technical Specs : Solubilizer in powder form; EXCiPACT
Ingredient(s) : Polysorbate 80
Dosage Form : Cream / Lotion / Ointment, Injectable / Parenteral
Grade : Topical, Parenteral
Category : Parenteral, Topical
Application : Topical
Excipient Details : Boric acid is used as an antimicrobial preservative in topical formulations such as creams and ointments.
Pharmacopoeia Ref : EP
Technical Specs : 99.9 % Boric Acid (H3BO3)
Ingredient(s) : Boric Acid Excipient
Dosage Form : Capsule, Cream / Lotion / Ointment, Emulsion, Gel, Injectable / Parenteral, Suspension, Tablet
Grade : Parenteral, Oral, Topical
Category : Emulsifying Agents, Film Formers & Plasticizers, Parenteral, Solubilizers, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Application : Emulsifying Agents, Film Formers & Plasticizers, Parenteral, Solubilizers, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Excipient Details : Polysorbate 80 is used as a plasticizer, solubilizer, emulsifier, surfactant, and suspension stabilizer. It is also used in parenteral products.
Dosage Form : Cream / Lotion / Ointment, Emulsion, Injectable / Parenteral, Softgels, Tablet
Grade : Oral, Topical, Parenteral
Category : Film Formers & Plasticizers, Parenteral, Topical
Application : Topical
Excipient Details : Menthol is used in nasal sprays, topical gel patches and creams, and ointments.
Dosage Form : Capsule, Cream / Lotion / Ointment, Suspension, Tablet
Grade : Oral, Topical & Parenteral
Category : Solubilizers, Surfactant & Foaming Agents
Application : Solubilizers, Surfactant & Foaming Agents
Excipient Details : Polysorbate 80 acts as solubilizer, emulsifier and wetting agent.
Dosage Form : Capsule, Cream / Lotion / Ointment, Emulsion, Gel, Paste, Shampoo, Solution, Syrup, Tablet
Grade : Topical, Oral
Category : Film Formers & Plasticizers, Solubilizers, Surfactant & Foaming Agents, Topical
Brand Name : MONTANOX 80 PHA PREMIUM
Application : Film Formers & Plasticizers, Solubilizers, Surfactant & Foaming Agents, Topical
Excipient Details : Non-Ionic Hydrophilic Surfactant, Emulsifier, Solubilizer
Pharmacopoeia Ref : Ph.Eur, USP-NF
Technical Specs : HLB: 15, EO: 20; EXCiPACT
Ingredient(s) : Polysorbate 80
Dosage Form : Capsule, Cream / Lotion / Ointment, Tablet
Grade : Oral, Topical
Category : Emulsifying Agents, Solubilizers, Surfactant & Foaming Agents, Topical
Brand Name : MONTANOX 80 PHA PREMIUM
Application : Emulsifying Agents, Solubilizers, Surfactant & Foaming Agents, Topical
Pharmacopoeia Ref : USP-NF, EP, JP
Technical Specs : Non-Ionic Hydrophilic surfactant, Emulsifier (o/w emulsion), Solu...
Ingredient(s) : Polysorbate 80
Dosage Form : Cream / Lotion / Ointment, Emulsion, Gel, Softgel Capsule
Grade : Not Available
Category : Thickeners and Stabilizers, Topical
Application : Thickeners and Stabilizers, Topical
Excipient Details : Structure-building consistency factor with dry feel, forms crystalline barrier on skin
Pharmacopoeia Ref : Ph. Eur., USP-NF, JP: Stearic ...
Technical Specs : Not Available
Ingredient(s) : Stearic Acid
Dosage Form : Cream / Lotion / Ointment, Emulsion, Gel
Grade : Topical
Category : Rheology Modifiers, Thickeners and Stabilizers, Topical
Application : Rheology Modifiers, Thickeners and Stabilizers, Topical
Excipient Details : Thickener, Stabilizer / Emulsifier, Texturizing Agent
Pharmacopoeia Ref : IID
Technical Specs : EXCiPACT
Ingredient(s) : Acrylamide / Sodium Acryloyldimethyl Taurate Copolymer Isohexadecane and Polysorbate 80
Global Sales Information
Market Place
Patents & EXCLUSIVITIES
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
26
PharmaCompass offers a list of Zinc Sulphate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Zinc Sulphate manufacturer or Zinc Sulphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zinc Sulphate manufacturer or Zinc Sulphate supplier.
PharmaCompass also assists you with knowing the Zinc Sulphate API Price utilized in the formulation of products. Zinc Sulphate API Price is not always fixed or binding as the Zinc Sulphate Price is obtained through a variety of data sources. The Zinc Sulphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zinc Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinc Sulphate, including repackagers and relabelers. The FDA regulates Zinc Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinc Sulphate 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 Zinc Sulphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinc Sulphate supplier is an individual or a company that provides Zinc Sulphate active pharmaceutical ingredient (API) or Zinc Sulphate finished formulations upon request. The Zinc Sulphate suppliers may include Zinc Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Zinc Sulphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zinc Sulphate DMF (Drug Master File) is a document detailing the whole manufacturing process of Zinc Sulphate active pharmaceutical ingredient (API) in detail. Different forms of Zinc Sulphate DMFs exist exist since differing nations have different regulations, such as Zinc Sulphate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zinc Sulphate DMF submitted to regulatory agencies in the US is known as a USDMF. Zinc Sulphate USDMF includes data on Zinc Sulphate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zinc Sulphate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zinc Sulphate suppliers with USDMF on PharmaCompass.
Zinc Sulphate 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 Zinc Sulphate GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Zinc Sulphate GMP manufacturer or Zinc Sulphate GMP API supplier for your needs.
A Zinc Sulphate CoA (Certificate of Analysis) is a formal document that attests to Zinc Sulphate's compliance with Zinc Sulphate specifications and serves as a tool for batch-level quality control.
Zinc Sulphate CoA mostly includes findings from lab analyses of a specific batch. For each Zinc Sulphate 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.
Zinc Sulphate may be tested according to a variety of international standards, such as European Pharmacopoeia (Zinc Sulphate EP), Zinc Sulphate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zinc Sulphate USP).