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01 1M/s mylan laboratories Limited
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01 1Tenofovir Disoproxil Maleate IH
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01 1WC-0359
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01 1India
Tenofovir Disoproxil Maleate IH
Date of Issue : 2019-05-21
Valid Till : 2022-05-20
Written Confirmation Number : WC-0359
Address of the Firm : Unit 10-Plot No.86 Ramky Pharma City India Ltd SEZ, Jawaharlal nehru pharma City...
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A Tenofovir Disoproxil Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenofovir Disoproxil Maleate, including repackagers and relabelers. The FDA regulates Tenofovir Disoproxil Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenofovir Disoproxil Maleate 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 Tenofovir Disoproxil Maleate supplier is an individual or a company that provides Tenofovir Disoproxil Maleate active pharmaceutical ingredient (API) or Tenofovir Disoproxil Maleate finished formulations upon request. The Tenofovir Disoproxil Maleate suppliers may include Tenofovir Disoproxil Maleate API manufacturers, exporters, distributors and traders.
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A Tenofovir Disoproxil Maleate written confirmation (Tenofovir Disoproxil Maleate WC) is an official document issued by a regulatory agency to a Tenofovir Disoproxil Maleate manufacturer, verifying that the manufacturing facility of a Tenofovir Disoproxil Maleate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tenofovir Disoproxil Maleate APIs or Tenofovir Disoproxil Maleate finished pharmaceutical products to another nation, regulatory agencies frequently require a Tenofovir Disoproxil Maleate WC (written confirmation) as part of the regulatory process.
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