01 1M/s Glenmark Life Sciences Limited
01 1Moexipril Hydrochloride IH
01 1WC-0057n
01 1India
Date of Issue : 2022-06-07
Valid Till : 2025-06-25
Written Confirmation Number : WC-0057n
Address of the Firm : Plot No. 3109, GIDC, Industrial Estate, Ankleshwar-393 002, Bharuch, Gujarat
A Moexipril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Moexipril, including repackagers and relabelers. The FDA regulates Moexipril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Moexipril 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 Moexipril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Moexipril supplier is an individual or a company that provides Moexipril active pharmaceutical ingredient (API) or Moexipril finished formulations upon request. The Moexipril suppliers may include Moexipril API manufacturers, exporters, distributors and traders.
click here to find a list of Moexipril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Moexipril written confirmation (Moexipril WC) is an official document issued by a regulatory agency to a Moexipril manufacturer, verifying that the manufacturing facility of a Moexipril active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Moexipril APIs or Moexipril finished pharmaceutical products to another nation, regulatory agencies frequently require a Moexipril WC (written confirmation) as part of the regulatory process.
click here to find a list of Moexipril suppliers with Written Confirmation (WC) on PharmaCompass.
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