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Molecular Weight | 215.21 g/mol |
---|---|
Molecular Formula | C11H9N3O2 |
XLogP3 | 1.3 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 1 |
Exact Mass | 215.069476538 g/mol |
Monoisotopic Mass | 215.069476538 g/mol |
Topological Polar Surface Area | 84.6 A^2 |
Heavy Atom Count | 16 |
Formal Charge | 0 |
Complexity | 373 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Global Sales Information
ABOUT THIS PAGE
A Naftazone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naftazone, including repackagers and relabelers. The FDA regulates Naftazone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naftazone 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 Naftazone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naftazone supplier is an individual or a company that provides Naftazone active pharmaceutical ingredient (API) or Naftazone finished formulations upon request. The Naftazone suppliers may include Naftazone API manufacturers, exporters, distributors and traders.
click here to find a list of Naftazone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Naftazone 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 Naftazone 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 Naftazone GMP manufacturer or Naftazone GMP API supplier for your needs.
A Naftazone CoA (Certificate of Analysis) is a formal document that attests to Naftazone's compliance with Naftazone specifications and serves as a tool for batch-level quality control.
Naftazone CoA mostly includes findings from lab analyses of a specific batch. For each Naftazone 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.
Naftazone may be tested according to a variety of international standards, such as European Pharmacopoeia (Naftazone EP), Naftazone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Naftazone USP).
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