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
A Tenofovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenofovir, including repackagers and relabelers. The FDA regulates Tenofovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenofovir 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 Tenofovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenofovir supplier is an individual or a company that provides Tenofovir active pharmaceutical ingredient (API) or Tenofovir finished formulations upon request. The Tenofovir suppliers may include Tenofovir API manufacturers, exporters, distributors and traders.
click here to find a list of Tenofovir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tenofovir written confirmation (Tenofovir WC) is an official document issued by a regulatory agency to a Tenofovir manufacturer, verifying that the manufacturing facility of a Tenofovir active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tenofovir APIs or Tenofovir finished pharmaceutical products to another nation, regulatory agencies frequently require a Tenofovir WC (written confirmation) as part of the regulatory process.
click here to find a list of Tenofovir suppliers with Written Confirmation (WC) on PharmaCompass.
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