01 1Dishman Carbogen Amcis Limited
02 1M/s. Dishman Pharmaceuticals and Chemicals Ltd.
03 1M/s. Hetero Drugs Limited, Unit -I
04 1M/s. Unichem Lab. Ltd.
01 1Eprosartan Mesylate (IH)
02 3Eprosartan Mesylate IH
01 1WC-0040
02 1WC-0062
03 1WC-0135
04 1WC-0135A
01 4India
Date of Issue : 2019-12-03
Valid Till : 2022-07-21
Written Confirmation Number : WC-0135A
Address of the Firm : Survey No. 47, Paiki Sub Plot No. 1, Village Lodariyal, Taluka Sanand, Dist. Ahm...
Date of Issue : 2019-07-22
Valid Till : 2022-07-02
Written Confirmation Number : WC-0135
Address of the Firm : Survey No. 47, Paiki Sub Plot No. 1, Village Lodariyal, Taluka Sanand, Dist. Ahm...
Date of Issue : 2022-07-04
Valid Till : 2025-07-03
Written Confirmation Number : WC-0040
Address of the Firm : Unit-I, Survey No.213, 214 & 255, Bonthapally Village, Jinnaram Mandal, Medak ...
Date of Issue : 2022-06-17
Valid Till : 2025-07-21
Written Confirmation Number : WC-0062
Address of the Firm : Plot No.197, Sector 1, Pithampur, Dist. Dhar, M.P
38
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A Teveten manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Teveten, including repackagers and relabelers. The FDA regulates Teveten manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Teveten 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 Teveten supplier is an individual or a company that provides Teveten active pharmaceutical ingredient (API) or Teveten finished formulations upon request. The Teveten suppliers may include Teveten API manufacturers, exporters, distributors and traders.
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A Teveten written confirmation (Teveten WC) is an official document issued by a regulatory agency to a Teveten manufacturer, verifying that the manufacturing facility of a Teveten active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Teveten APIs or Teveten finished pharmaceutical products to another nation, regulatory agencies frequently require a Teveten WC (written confirmation) as part of the regulatory process.
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