01 1Alps Pharmaceutical Co., Ltd.
02 1Chifeng Arker Pharmaceutical Technology Co. , Ltd.
03 1Divi's Laboratories Limited
04 2F. Hoffmann-La Roche Limited.
05 2Wockhardt Limited
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PharmaCompass offers a list of Dextromethorphan Hydrobromide 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 Hydrobromide manufacturer or Dextromethorphan Hydrobromide supplier for your needs.
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PharmaCompass also assists you with knowing the Dextromethorphan Hydrobromide API Price utilized in the formulation of products. Dextromethorphan Hydrobromide API Price is not always fixed or binding as the Dextromethorphan Hydrobromide Price is obtained through a variety of data sources. The Dextromethorphan Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PROMETHAZINE DM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PROMETHAZINE DM, including repackagers and relabelers. The FDA regulates PROMETHAZINE DM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PROMETHAZINE 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 PROMETHAZINE DM supplier is an individual or a company that provides PROMETHAZINE DM active pharmaceutical ingredient (API) or PROMETHAZINE DM finished formulations upon request. The PROMETHAZINE DM suppliers may include PROMETHAZINE DM API manufacturers, exporters, distributors and traders.
click here to find a list of PROMETHAZINE DM suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The PROMETHAZINE DM Drug Master File in Japan (PROMETHAZINE DM JDMF) empowers PROMETHAZINE DM API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the PROMETHAZINE DM JDMF during the approval evaluation for pharmaceutical products. At the time of PROMETHAZINE DM JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of PROMETHAZINE DM suppliers with JDMF on PharmaCompass.
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