01 1M/s Hetero Drugs Limited
02 1M/s Mangalam Drugs and Organics Ltd
03 1M/s S.M.S Pharmaceuticals Ltd
04 1M/s mylan laboratories Limited
05 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
06 1M/s. Cipla Ltd
07 1M/s. Cipla Ltd.
08 1M/s. Dasami Lab Private Limited
09 1M/s. Hetero Labs Limited.,
10 1M/s. Hetro Labs Limited
11 1M/s. Laurus Labs Pvt. Ltd.,
12 1M/s. Lupin Ltd
13 1M/s. Macleods Pharmaceuticals Ltd.
14 1M/s. Mangalam Drugs & Organics Ltd., Unit-2
15 2M/s. Mylan Laboratories Ltd.,
16 1M/s. Shilpa Medicare Ltd.,
17 1M/s. Unimark Remedies Limited
18 1M/sTyche Industries Limited
19 1Solara Active Pharma Sciences Limited
A Tenofovir Disoproxil Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenofovir Disoproxil Fumarate, including repackagers and relabelers. The FDA regulates Tenofovir Disoproxil Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenofovir Disoproxil Fumarate 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 Fumarate supplier is an individual or a company that provides Tenofovir Disoproxil Fumarate active pharmaceutical ingredient (API) or Tenofovir Disoproxil Fumarate finished formulations upon request. The Tenofovir Disoproxil Fumarate suppliers may include Tenofovir Disoproxil Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Tenofovir Disoproxil Fumarate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tenofovir Disoproxil Fumarate written confirmation (Tenofovir Disoproxil Fumarate WC) is an official document issued by a regulatory agency to a Tenofovir Disoproxil Fumarate manufacturer, verifying that the manufacturing facility of a Tenofovir Disoproxil Fumarate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tenofovir Disoproxil Fumarate APIs or Tenofovir Disoproxil Fumarate finished pharmaceutical products to another nation, regulatory agencies frequently require a Tenofovir Disoproxil Fumarate WC (written confirmation) as part of the regulatory process.
click here to find a list of Tenofovir Disoproxil Fumarate suppliers with Written Confirmation (WC) on PharmaCompass.
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