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1. 22306-37-2
2. Bismuth(iii) Acetate
3. Bismuth Triacetate
4. Bismuth;triacetate
5. 8aja86y692
6. Mfcd00015629
7. 29094-03-9
8. Acetic Acid, Bismuth Salt
9. Unii-8aja86y692
10. Acetic Acid, Bismuth(3+) Salt
11. Hsdb 2186
12. Bismuth(iii)acetate
13. Einecs 244-904-5
14. Einecs 249-426-0
15. Nsc 370498
16. Trisacetic Acid Bismuth Salt
17. Dtxsid101043458
18. Akos015915836
19. Ft-0725987
20. D70195
| Molecular Weight | 386.11 g/mol |
|---|---|
| Molecular Formula | C6H9BiO6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 0 |
| Exact Mass | 386.02031 g/mol |
| Monoisotopic Mass | 386.02031 g/mol |
| Topological Polar Surface Area | 120 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 25.5 |
| 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 | 4 |
ABOUT THIS PAGE
A Bismuth Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bismuth Acetate, including repackagers and relabelers. The FDA regulates Bismuth Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bismuth Acetate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Bismuth Acetate supplier is an individual or a company that provides Bismuth Acetate active pharmaceutical ingredient (API) or Bismuth Acetate finished formulations upon request. The Bismuth Acetate suppliers may include Bismuth Acetate API manufacturers, exporters, distributors and traders.
Bismuth Acetate 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 Bismuth Acetate 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 Bismuth Acetate GMP manufacturer or Bismuth Acetate GMP API supplier for your needs.
A Bismuth Acetate CoA (Certificate of Analysis) is a formal document that attests to Bismuth Acetate's compliance with Bismuth Acetate specifications and serves as a tool for batch-level quality control.
Bismuth Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Bismuth Acetate 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.
Bismuth Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Bismuth Acetate EP), Bismuth Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Bismuth Acetate USP).
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