Temad- We think of world-class quality.
01 1TEMAD CO ACTIVE PHARMACEUTICAL INGREDIENTS
02 1DIVI'S LABORATORIES LIMITED
01 1Dextromethorphan base
02 1Japanese Pharmacy Hydrofluoric Acid Dextromethorphan
01 1India
02 1Iran
Temad- We think of world-class quality.
Dextromethorphan Hydrobromide, Japanese Pharmacopoeia
Registration Number : 219MF10366
Registrant's Address : No. 3 Bisotown St. Fatemi Sq. Tehran,Iran
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2007-12-13
Registration Number : 220MF10194
Registrant's Address : 1-72/23(P)/DIVIS/303, Divi Towers, Cyber Hills, Gachibowli, Hyderabad-500 032, ...
Initial Date of Registration : 2008-08-28
Latest Date of Registration : 2022-09-08
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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.
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 Koffex DM Drug Master File in Japan (Koffex DM JDMF) empowers Koffex 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 Koffex DM JDMF during the approval evaluation for pharmaceutical products. At the time of Koffex 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 Koffex DM suppliers with JDMF on PharmaCompass.
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