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1. Schembl718621
2. Akos015896474
| Molecular Weight | 483.5 g/mol |
|---|---|
| Molecular Formula | C20H22N5NaO6S |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 5 |
| Exact Mass | 483.11884889 g/mol |
| Monoisotopic Mass | 483.11884889 g/mol |
| Topological Polar Surface Area | 176 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 851 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A Azlocillin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azlocillin Sodium, including repackagers and relabelers. The FDA regulates Azlocillin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azlocillin Sodium 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 Azlocillin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azlocillin Sodium supplier is an individual or a company that provides Azlocillin Sodium active pharmaceutical ingredient (API) or Azlocillin Sodium finished formulations upon request. The Azlocillin Sodium suppliers may include Azlocillin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Azlocillin Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Azlocillin Sodium 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 Azlocillin Sodium 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 Azlocillin Sodium GMP manufacturer or Azlocillin Sodium GMP API supplier for your needs.
A Azlocillin Sodium CoA (Certificate of Analysis) is a formal document that attests to Azlocillin Sodium's compliance with Azlocillin Sodium specifications and serves as a tool for batch-level quality control.
Azlocillin Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Azlocillin Sodium 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.
Azlocillin Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Azlocillin Sodium EP), Azlocillin Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Azlocillin Sodium USP).
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