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1. 7446-19-7
2. 16788-42-4
3. Zinc Sulphate Monohydrate
4. Zinc;sulfate;hydrate
5. Zincaps
6. Zincsulfatemonohydrate
7. Solvazinc; Solvezink
8. Sulfuric Acid, Zinc Salt (1:1), Monohydrate
9. Ptx099xsf1
10. Sulfuric Acid, Zinc Salt (1:1), Hydrate (8ci,9ci)
11. Mfcd00149893
12. Zinc Sulfate Hydrate, Puratronic , 99.999per Cent (metals Basis)
13. Unii-ptx099xsf1
14. Gunningite
15. Sulfato De Zinc Monohydratado
16. Zinc Sulfate (tn)
17. Zinc(ii)sulfatexhydrate
18. Zinc Sulfate-1-hydrate
19. Zinc Sulfate, Monohydrate
20. Zinc(ii) Sulfate Hydrate
21. Zinc(ii) Sulfate Xhydrate
22. Zinc Sulfate [who-ip]
23. Zinc Sulfate Monohydrate Powder
24. Dtxsid2035019
25. Zinc Sulfate Hydrate, Puratronic?
26. Zinc Sulfate (monohydrate)
27. Zinc Sulphate (monohydrate)
28. Zinc Sulfate Monohydrate [mi]
29. Zinc Sulfate Monohydrate, Zn 35.5%
30. Akos015855396
31. Zinc Sulfate Monohydrate [vandf]
32. Zinc Sulfate Monohydrate [who-dd]
33. Zinc Sulfate Monohydrate [who-ip]
34. Zinc Sulfate Monohydrate, P.a., 98.0%
35. Ft-0653225
36. D06371
37. Zinc Sulfate Monohydrate [ep Monograph]
38. Zinci Sulfas Monohydrate [who-ip Latin]
39. Zinc Sulfate Monohydrate [usp Monograph]
40. A838140
41. Q27286751
42. Zinc Sulfate Monohydrate, >=99.9% Trace Metals Basis
43. Zinc Sulfate Monohydrate, Purum P.a., >=99.0% (kt)
Molecular Weight | 179.5 g/mol |
---|---|
Molecular Formula | H2O5SZn |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 0 |
Exact Mass | 177.891436 g/mol |
Monoisotopic Mass | 177.891436 g/mol |
Topological Polar Surface Area | 89.6 Ų |
Heavy Atom Count | 7 |
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 | 3 |
NDC Package Code : 55570-540
Start Marketing Date : 2015-02-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67706-0007
Start Marketing Date : 2015-02-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1364
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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Application : Parenteral
Excipient Details : A & C's Glycerol multi-compendial is an excipient that meets USP-NF, EP and BP monographs.
Pharmacopoeia Ref : Multi-compendial
Technical Specs : Not Available
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Excipient Details : A & C's Glycerol is an excipient which meets the USP monograph.
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Excipient Details : A & C's Polysorbate 80 multi-compendial is an excipient which meets USP-NF, EP, BP and JP monographs.
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Pharmacopoeia Ref : EP/USP, USP/FCC
Technical Specs : Not Available
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Excipient Details : Act as a bulk sweetener and vehicle in liquid dosage forms and as a humectant in semi solids.
Pharmacopoeia Ref : EP/USP
Technical Specs : Not Available
Ingredient(s) : Sorbitol liquid crystallizing
Dosage Form : Injectable / Parenteral
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Ingredient(s) : Hydroxypropyl Pea Starch, Sorbitol, Titanium Dioxide, Stearic Acid
Excipients by Applications
Market Place
ABOUT THIS PAGE
A Zinc Sulfate Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinc Sulfate Monohydrate, including repackagers and relabelers. The FDA regulates Zinc Sulfate Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinc Sulfate Monohydrate 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 Sulfate Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinc Sulfate Monohydrate supplier is an individual or a company that provides Zinc Sulfate Monohydrate active pharmaceutical ingredient (API) or Zinc Sulfate Monohydrate finished formulations upon request. The Zinc Sulfate Monohydrate suppliers may include Zinc Sulfate Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Zinc Sulfate Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Zinc Sulfate Monohydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zinc Sulfate Monohydrate API and other APIs are published in this directory by the FDA.
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 Zinc Sulfate Monohydrate 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.
The NDC directory also contains data on finished compounded human drug products that contain Zinc Sulfate Monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zinc Sulfate Monohydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zinc Sulfate Monohydrate suppliers with NDC on PharmaCompass.
Zinc Sulfate Monohydrate 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 Sulfate Monohydrate 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 Sulfate Monohydrate GMP manufacturer or Zinc Sulfate Monohydrate GMP API supplier for your needs.
A Zinc Sulfate Monohydrate CoA (Certificate of Analysis) is a formal document that attests to Zinc Sulfate Monohydrate's compliance with Zinc Sulfate Monohydrate specifications and serves as a tool for batch-level quality control.
Zinc Sulfate Monohydrate CoA mostly includes findings from lab analyses of a specific batch. For each Zinc Sulfate Monohydrate 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 Sulfate Monohydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Zinc Sulfate Monohydrate EP), Zinc Sulfate Monohydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zinc Sulfate Monohydrate USP).
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