01 1M/s. Cipla Ltd.
01 1Tenofovir Hydrochloride (BP/Ph. Eur.)
01 1WC-0140
01 1India
Tenofovir Hydrochloride (BP/Ph. Eur.)
Date of Issue : 2022-06-03
Valid Till : 2025-07-02
Written Confirmation Number : WC-0140
Address of the Firm : D-22, MIDC, Kurkumbh, Dist. Pune-413 802
53
PharmaCompass offers a list of Tenofovir 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 Tenofovir manufacturer or Tenofovir supplier for your needs.
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PharmaCompass also assists you with knowing the Tenofovir API Price utilized in the formulation of products. Tenofovir API Price is not always fixed or binding as the Tenofovir Price is obtained through a variety of data sources. The Tenofovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tenefovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenefovir, including repackagers and relabelers. The FDA regulates Tenefovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenefovir 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 Tenefovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenefovir supplier is an individual or a company that provides Tenefovir active pharmaceutical ingredient (API) or Tenefovir finished formulations upon request. The Tenefovir suppliers may include Tenefovir API manufacturers, exporters, distributors and traders.
click here to find a list of Tenefovir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tenefovir written confirmation (Tenefovir WC) is an official document issued by a regulatory agency to a Tenefovir manufacturer, verifying that the manufacturing facility of a Tenefovir active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tenefovir APIs or Tenefovir finished pharmaceutical products to another nation, regulatory agencies frequently require a Tenefovir WC (written confirmation) as part of the regulatory process.
click here to find a list of Tenefovir suppliers with Written Confirmation (WC) on PharmaCompass.
