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1. Schembl1649371
2. Akos025402032
3. Ac-3448
| Molecular Weight | 478.4 g/mol |
|---|---|
| Molecular Formula | C24H29BrFNO3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Exact Mass | 477.13148 g/mol |
| Monoisotopic Mass | 477.13148 g/mol |
| Topological Polar Surface Area | 46.5 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 539 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A Flutropium bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flutropium bromide, including repackagers and relabelers. The FDA regulates Flutropium bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flutropium bromide 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 Flutropium bromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flutropium bromide supplier is an individual or a company that provides Flutropium bromide active pharmaceutical ingredient (API) or Flutropium bromide finished formulations upon request. The Flutropium bromide suppliers may include Flutropium bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Flutropium bromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Flutropium bromide 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 Flutropium bromide 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 Flutropium bromide GMP manufacturer or Flutropium bromide GMP API supplier for your needs.
A Flutropium bromide CoA (Certificate of Analysis) is a formal document that attests to Flutropium bromide's compliance with Flutropium bromide specifications and serves as a tool for batch-level quality control.
Flutropium bromide CoA mostly includes findings from lab analyses of a specific batch. For each Flutropium bromide 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.
Flutropium bromide may be tested according to a variety of international standards, such as European Pharmacopoeia (Flutropium bromide EP), Flutropium bromide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Flutropium bromide USP).
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