01 1M/s MSN Laboratories
02 1M/s. Sun Pharmaceuticals Ltd.
01 1TIAGABINE HYDROCHLORIDE USP
02 1Tiagabine Hydrochloride IH/USP
01 1WC-0168
02 1WC-0383A6
01 2India
Date of Issue : 2020-07-27
Valid Till : 2022-08-08
Written Confirmation Number : WC-0383A6
Address of the Firm : Sy. No.455/A, 455/AA, 455/E & 455/EE Chandampet Village Shankarampet Mandal Meda...
Tiagabine Hydrochloride IH/USP
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm : Plot No. 24/2, & 25, Phase -IV, GIDC, Industrial Zone, At & Post - Panoli, Dist....
A Tiagabine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiagabine Hydrochloride, including repackagers and relabelers. The FDA regulates Tiagabine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiagabine Hydrochloride 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 Tiagabine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tiagabine Hydrochloride supplier is an individual or a company that provides Tiagabine Hydrochloride active pharmaceutical ingredient (API) or Tiagabine Hydrochloride finished formulations upon request. The Tiagabine Hydrochloride suppliers may include Tiagabine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tiagabine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tiagabine Hydrochloride written confirmation (Tiagabine Hydrochloride WC) is an official document issued by a regulatory agency to a Tiagabine Hydrochloride manufacturer, verifying that the manufacturing facility of a Tiagabine Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tiagabine Hydrochloride APIs or Tiagabine Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Tiagabine Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Tiagabine Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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