Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1M/s.Granules India
02 1M/s. Laurus Labs Pvt. Ltd.,
01 1Tenofovir Disoproxil Succinate (IH)
02 1Tenofovir Disoproxil Succinate IH
01 1WC-0024
02 1WC-0213
01 2India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Tenofovir Disoproxil Succinate IH
Date of Issue : 2022-07-08
Valid Till : 2025-06-28
Written Confirmation Number : WC-0024
Address of the Firm : Plot No-8, Jawaharlal Nehru Pharamacity,Tadi (v), Parawada (M), Vishakapatnam Di...
Tenofovir Disoproxil Succinate (IH)
Date of Issue : 2023-07-03
Valid Till : 2025-07-02
Written Confirmation Number : WC-0213
Address of the Firm : Plot No.21, Jawaharlal Nehru Pharma City, Parawada MandaI, Visakhapatnam, Visakh...
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A Tenofovir Disoproxil Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenofovir Disoproxil Succinate, including repackagers and relabelers. The FDA regulates Tenofovir Disoproxil Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenofovir Disoproxil Succinate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tenofovir Disoproxil Succinate supplier is an individual or a company that provides Tenofovir Disoproxil Succinate active pharmaceutical ingredient (API) or Tenofovir Disoproxil Succinate finished formulations upon request. The Tenofovir Disoproxil Succinate suppliers may include Tenofovir Disoproxil Succinate API manufacturers, exporters, distributors and traders.
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A Tenofovir Disoproxil Succinate written confirmation (Tenofovir Disoproxil Succinate WC) is an official document issued by a regulatory agency to a Tenofovir Disoproxil Succinate manufacturer, verifying that the manufacturing facility of a Tenofovir Disoproxil Succinate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tenofovir Disoproxil Succinate APIs or Tenofovir Disoproxil Succinate finished pharmaceutical products to another nation, regulatory agencies frequently require a Tenofovir Disoproxil Succinate WC (written confirmation) as part of the regulatory process.
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