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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - TABLET;ORAL - EQ 250MG BASE;12.5MG, ...DOSAGE - TABLET;ORAL - EQ 250MG BASE;12.5MG, 75MG, 50MG
USFDA APPLICATION NUMBER - 206619
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 2...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 208624
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ABOUT THIS PAGE
A Dasabuvir Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dasabuvir Sodium, including repackagers and relabelers. The FDA regulates Dasabuvir Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dasabuvir 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 Dasabuvir Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dasabuvir Sodium supplier is an individual or a company that provides Dasabuvir Sodium active pharmaceutical ingredient (API) or Dasabuvir Sodium finished formulations upon request. The Dasabuvir Sodium suppliers may include Dasabuvir Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Dasabuvir Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Dasabuvir 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 Dasabuvir 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 Dasabuvir Sodium GMP manufacturer or Dasabuvir Sodium GMP API supplier for your needs.
A Dasabuvir Sodium CoA (Certificate of Analysis) is a formal document that attests to Dasabuvir Sodium's compliance with Dasabuvir Sodium specifications and serves as a tool for batch-level quality control.
Dasabuvir Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Dasabuvir 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.
Dasabuvir Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Dasabuvir Sodium EP), Dasabuvir Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dasabuvir Sodium USP).
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