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Looking for 161814-49-9 / Amprenavir API manufacturers, exporters & distributors?

Amprenavir manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Amprenavir 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 Amprenavir manufacturer or Amprenavir supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amprenavir manufacturer or Amprenavir supplier.

PharmaCompass also assists you with knowing the Amprenavir API Price utilized in the formulation of products. Amprenavir API Price is not always fixed or binding as the Amprenavir Price is obtained through a variety of data sources. The Amprenavir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Amprenavir

Synonyms

161814-49-9, Agenerase, Prozei, Vx-478, 141w94, Kvx-478

Cas Number

161814-49-9

Unique Ingredient Identifier (UNII)

5S0W860XNR

About Amprenavir

Amprenavir is a synthetic derivative of hydroxyethylamine sulfonamide that selectively binds to and inhibits human immunodeficiency virus (HIV) protease.

Amprenavir Manufacturers

A Amprenavir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amprenavir, including repackagers and relabelers. The FDA regulates Amprenavir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amprenavir API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Amprenavir Suppliers

A Amprenavir supplier is an individual or a company that provides Amprenavir active pharmaceutical ingredient (API) or Amprenavir finished formulations upon request. The Amprenavir suppliers may include Amprenavir API manufacturers, exporters, distributors and traders.

click here to find a list of Amprenavir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Amprenavir USDMF

A Amprenavir DMF (Drug Master File) is a document detailing the whole manufacturing process of Amprenavir active pharmaceutical ingredient (API) in detail. Different forms of Amprenavir DMFs exist exist since differing nations have different regulations, such as Amprenavir USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Amprenavir DMF submitted to regulatory agencies in the US is known as a USDMF. Amprenavir USDMF includes data on Amprenavir's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Amprenavir USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Amprenavir suppliers with USDMF on PharmaCompass.

Amprenavir GMP

Amprenavir 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 Amprenavir 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 Amprenavir GMP manufacturer or Amprenavir GMP API supplier for your needs.

Amprenavir CoA

A Amprenavir CoA (Certificate of Analysis) is a formal document that attests to Amprenavir's compliance with Amprenavir specifications and serves as a tool for batch-level quality control.

Amprenavir CoA mostly includes findings from lab analyses of a specific batch. For each Amprenavir 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.

Amprenavir may be tested according to a variety of international standards, such as European Pharmacopoeia (Amprenavir EP), Amprenavir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Amprenavir USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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