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![Pentazocine Hydrochloride [Usan]](https://www.pharmacompass.com/image/drug/107799.png)
| Molecular Weight | 321.9 g/mol |
|---|---|
| Molecular Formula | C19H28ClNO |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 321.1859422 g/mol |
| Monoisotopic Mass | 321.1859422 g/mol |
| Topological Polar Surface Area | 23.5 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 414 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A Pentazocine Hydrochloride [Usan] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentazocine Hydrochloride [Usan], including repackagers and relabelers. The FDA regulates Pentazocine Hydrochloride [Usan] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentazocine Hydrochloride [Usan] 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 Pentazocine Hydrochloride [Usan] supplier is an individual or a company that provides Pentazocine Hydrochloride [Usan] active pharmaceutical ingredient (API) or Pentazocine Hydrochloride [Usan] finished formulations upon request. The Pentazocine Hydrochloride [Usan] suppliers may include Pentazocine Hydrochloride [Usan] API manufacturers, exporters, distributors and traders.
Pentazocine Hydrochloride [Usan] 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 Pentazocine Hydrochloride [Usan] 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 Pentazocine Hydrochloride [Usan] GMP manufacturer or Pentazocine Hydrochloride [Usan] GMP API supplier for your needs.
A Pentazocine Hydrochloride [Usan] CoA (Certificate of Analysis) is a formal document that attests to Pentazocine Hydrochloride [Usan]'s compliance with Pentazocine Hydrochloride [Usan] specifications and serves as a tool for batch-level quality control.
Pentazocine Hydrochloride [Usan] CoA mostly includes findings from lab analyses of a specific batch. For each Pentazocine Hydrochloride [Usan] 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.
Pentazocine Hydrochloride [Usan] may be tested according to a variety of international standards, such as European Pharmacopoeia (Pentazocine Hydrochloride [Usan] EP), Pentazocine Hydrochloride [Usan] JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pentazocine Hydrochloride [Usan] USP).
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