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 Dextromethorphanum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextromethorphanum, including repackagers and relabelers. The FDA regulates Dextromethorphanum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextromethorphanum 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 Dextromethorphanum supplier is an individual or a company that provides Dextromethorphanum active pharmaceutical ingredient (API) or Dextromethorphanum finished formulations upon request. The Dextromethorphanum suppliers may include Dextromethorphanum API manufacturers, exporters, distributors and traders.
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A Dextromethorphanum written confirmation (Dextromethorphanum WC) is an official document issued by a regulatory agency to a Dextromethorphanum manufacturer, verifying that the manufacturing facility of a Dextromethorphanum active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dextromethorphanum APIs or Dextromethorphanum finished pharmaceutical products to another nation, regulatory agencies frequently require a Dextromethorphanum WC (written confirmation) as part of the regulatory process.
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