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INTERMEDIATES SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - TABLET;ORAL - 12.5MG;75MG;50MG **Fed...DOSAGE - TABLET;ORAL - 12.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 207931
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RELEASE;ORAL - EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 Paritaprevir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paritaprevir, including repackagers and relabelers. The FDA regulates Paritaprevir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paritaprevir 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 Paritaprevir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Paritaprevir supplier is an individual or a company that provides Paritaprevir active pharmaceutical ingredient (API) or Paritaprevir finished formulations upon request. The Paritaprevir suppliers may include Paritaprevir API manufacturers, exporters, distributors and traders.
click here to find a list of Paritaprevir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Paritaprevir 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 Paritaprevir 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 Paritaprevir GMP manufacturer or Paritaprevir GMP API supplier for your needs.
A Paritaprevir CoA (Certificate of Analysis) is a formal document that attests to Paritaprevir's compliance with Paritaprevir specifications and serves as a tool for batch-level quality control.
Paritaprevir CoA mostly includes findings from lab analyses of a specific batch. For each Paritaprevir 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.
Paritaprevir may be tested according to a variety of international standards, such as European Pharmacopoeia (Paritaprevir EP), Paritaprevir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Paritaprevir USP).
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