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 Pertussin DM Extra Strength manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pertussin DM Extra Strength, including repackagers and relabelers. The FDA regulates Pertussin DM Extra Strength manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pertussin DM Extra Strength 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 Pertussin DM Extra Strength supplier is an individual or a company that provides Pertussin DM Extra Strength active pharmaceutical ingredient (API) or Pertussin DM Extra Strength finished formulations upon request. The Pertussin DM Extra Strength suppliers may include Pertussin DM Extra Strength API manufacturers, exporters, distributors and traders.
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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 Pertussin DM Extra Strength Drug Master File in Japan (Pertussin DM Extra Strength JDMF) empowers Pertussin DM Extra Strength 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 Pertussin DM Extra Strength JDMF during the approval evaluation for pharmaceutical products. At the time of Pertussin DM Extra Strength JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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