01 1M/s. Dishman Pharmaceuticals and Chemicals Ltd.
01 1Hexetidine Ph.Eur
01 1WC-0135
01 1India
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...
A Hexetidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexetidine, including repackagers and relabelers. The FDA regulates Hexetidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexetidine 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 Hexetidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexetidine supplier is an individual or a company that provides Hexetidine active pharmaceutical ingredient (API) or Hexetidine finished formulations upon request. The Hexetidine suppliers may include Hexetidine API manufacturers, exporters, distributors and traders.
click here to find a list of Hexetidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hexetidine written confirmation (Hexetidine WC) is an official document issued by a regulatory agency to a Hexetidine manufacturer, verifying that the manufacturing facility of a Hexetidine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Hexetidine APIs or Hexetidine finished pharmaceutical products to another nation, regulatory agencies frequently require a Hexetidine WC (written confirmation) as part of the regulatory process.
click here to find a list of Hexetidine suppliers with Written Confirmation (WC) on PharmaCompass.
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