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PharmaCompass offers a list of Indinavir API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Indinavir manufacturer or Indinavir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Indinavir manufacturer or Indinavir supplier.
PharmaCompass also assists you with knowing the Indinavir API Price utilized in the formulation of products. Indinavir API Price is not always fixed or binding as the Indinavir Price is obtained through a variety of data sources. The Indinavir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Indinavir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Indinavir, including repackagers and relabelers. The FDA regulates Indinavir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Indinavir 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 Indinavir supplier is an individual or a company that provides Indinavir active pharmaceutical ingredient (API) or Indinavir finished formulations upon request. The Indinavir suppliers may include Indinavir API manufacturers, exporters, distributors and traders.
click here to find a list of Indinavir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Indinavir DMF (Drug Master File) is a document detailing the whole manufacturing process of Indinavir active pharmaceutical ingredient (API) in detail. Different forms of Indinavir DMFs exist exist since differing nations have different regulations, such as Indinavir USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Indinavir DMF submitted to regulatory agencies in the US is known as a USDMF. Indinavir USDMF includes data on Indinavir's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Indinavir USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Indinavir suppliers with USDMF on PharmaCompass.
Indinavir 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 Indinavir 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 Indinavir GMP manufacturer or Indinavir GMP API supplier for your needs.
A Indinavir CoA (Certificate of Analysis) is a formal document that attests to Indinavir's compliance with Indinavir specifications and serves as a tool for batch-level quality control.
Indinavir CoA mostly includes findings from lab analyses of a specific batch. For each Indinavir 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.
Indinavir may be tested according to a variety of international standards, such as European Pharmacopoeia (Indinavir EP), Indinavir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Indinavir USP).
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