01 1Divi’s Laboratories
01 1Dextromethorphan (USP)
01 1WC-0031
01 1India
Date of Issue : 2022-06-16
Valid Till : 2025-06-16
Written Confirmation Number : WC-0031
Address of the Firm : Unit-Lingojigudem (V) Choutuppal (M) Nalgonda District Talangana State India
40
PharmaCompass offers a list of Dextromethorphan API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Dextromethorphan manufacturer or Dextromethorphan supplier for your needs.
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PharmaCompass also assists you with knowing the Dextromethorphan API Price utilized in the formulation of products. Dextromethorphan API Price is not always fixed or binding as the Dextromethorphan Price is obtained through a variety of data sources. The Dextromethorphan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Demorphine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Demorphine, including repackagers and relabelers. The FDA regulates Demorphine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Demorphine 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 Demorphine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Demorphine supplier is an individual or a company that provides Demorphine active pharmaceutical ingredient (API) or Demorphine finished formulations upon request. The Demorphine suppliers may include Demorphine API manufacturers, exporters, distributors and traders.
click here to find a list of Demorphine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Demorphine written confirmation (Demorphine WC) is an official document issued by a regulatory agency to a Demorphine manufacturer, verifying that the manufacturing facility of a Demorphine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Demorphine APIs or Demorphine finished pharmaceutical products to another nation, regulatory agencies frequently require a Demorphine WC (written confirmation) as part of the regulatory process.
click here to find a list of Demorphine suppliers with Written Confirmation (WC) on PharmaCompass.
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