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 Koffex DM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Koffex DM, including repackagers and relabelers. The FDA regulates Koffex DM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Koffex DM API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Koffex DM supplier is an individual or a company that provides Koffex DM active pharmaceutical ingredient (API) or Koffex DM finished formulations upon request. The Koffex DM suppliers may include Koffex DM API manufacturers, exporters, distributors and traders.
click here to find a list of Koffex DM suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Koffex DM written confirmation (Koffex DM WC) is an official document issued by a regulatory agency to a Koffex DM manufacturer, verifying that the manufacturing facility of a Koffex DM active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Koffex DM APIs or Koffex DM finished pharmaceutical products to another nation, regulatory agencies frequently require a Koffex DM WC (written confirmation) as part of the regulatory process.
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