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
01 1Dextromethorphan hydrobromic acid hydrate
02 1Dextromethorphan hydrobromide Dextromethorphan Hy drobromide
03 2Dextromethorphan hydrobromide hydrate
04 1Japanese Pharmacopoeia dextromethorphan hydrobromide (production only)
05 2Japanese Pharmacopoeia dextromethorphan hydrobromide hydrate
01 1China
02 3India
03 1Japan
04 2Switzerland
Japanese Pharmacopoeia Dextromethorphan Hydrobromide Hydrate
Registration Number : 220MF10121
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2008-04-28
Latest Date of Registration : 2022-10-05
Dextromethorphan hydrobromide hydrate
Registration Number : 302MF10047
Registrant's Address : No. 8 Mysun Street, Hongshan Economic Development Zone, Chifeng, Inner Mongolia, Chin...
Initial Date of Registration : 2020-04-17
Latest Date of Registration : 2020-04-17
Japanese Pharmacopoeia Dextromethorphan Hydrobromide (for manufacturing purposes only)
Registration Number : 217MF10567
Registrant's Address : Divi Towers, 7-1-77/E/1/303, Dharam Karan Road, Ameerpet, Hyderabad-500 016, India
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2006-12-27
Registration Number : 218MF10104
Registrant's Address : Grenzacherstrasse 124, 4070 Basel, Switzerland
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2006-09-22
Japanese Pharmacopoeia Dextromethorphan Hydrobromide Hydrate
Registration Number : 219MF10119
Registrant's Address : Grenzacherstrasse 124, 4070 Basel, Switzerland
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2007-03-23
Dextromethorphan hydrobromide hydrate
Registration Number : 303MF10152
Registrant's Address : Wockhardt Towers, Bandra-kurla Complex, Bandra (East), Mumbai-400 051, Maharashtra, I...
Initial Date of Registration : 2021-09-28
Latest Date of Registration : 2021-09-28
Dextromethorphan hydrobromide hydrate
Registration Number : 220MF10108
Registrant's Address : Wockhardt Towers, Bandra-kurla Complex, Bandra (East), Mumbai-400 051, Maharashtra, I...
Initial Date of Registration : 2008-04-11
Latest Date of Registration : 2008-04-11
A Dextromethorphan Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextromethorphan Hydrobromide, including repackagers and relabelers. The FDA regulates Dextromethorphan Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextromethorphan Hydrobromide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Dextromethorphan Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dextromethorphan Hydrobromide supplier is an individual or a company that provides Dextromethorphan Hydrobromide active pharmaceutical ingredient (API) or Dextromethorphan Hydrobromide finished formulations upon request. The Dextromethorphan Hydrobromide suppliers may include Dextromethorphan Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Dextromethorphan Hydrobromide 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 Dextromethorphan Hydrobromide Drug Master File in Japan (Dextromethorphan Hydrobromide JDMF) empowers Dextromethorphan Hydrobromide 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 Dextromethorphan Hydrobromide JDMF during the approval evaluation for pharmaceutical products. At the time of Dextromethorphan Hydrobromide 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 Dextromethorphan Hydrobromide suppliers with JDMF on PharmaCompass.
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