01 1M/s Bajai Healthcare Limited
02 1M/s. Dishman Pharmaceuticals and Chemicals Ltd.
01 1Octenidine Dihydrochloride IH
02 1Octenidine Hydrochloride IH
01 1WC-0135
02 1WC-0277A5
01 2India
Date of Issue : 2021-12-16
Valid Till : 2024-06-14
Written Confirmation Number : WC-0277A5
Address of the Firm : Unit -2, Block No.588, Savli Karachia Road, At & Post- Gothada, Dist Vadodara, G...
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 Octenidine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Octenidine Dihydrochloride, including repackagers and relabelers. The FDA regulates Octenidine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Octenidine Dihydrochloride 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 Octenidine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Octenidine Dihydrochloride supplier is an individual or a company that provides Octenidine Dihydrochloride active pharmaceutical ingredient (API) or Octenidine Dihydrochloride finished formulations upon request. The Octenidine Dihydrochloride suppliers may include Octenidine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Octenidine Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Octenidine Dihydrochloride written confirmation (Octenidine Dihydrochloride WC) is an official document issued by a regulatory agency to a Octenidine Dihydrochloride manufacturer, verifying that the manufacturing facility of a Octenidine Dihydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Octenidine Dihydrochloride APIs or Octenidine Dihydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Octenidine Dihydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Octenidine Dihydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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