01 1Cheer Fine Pharmaceutical Co. , Ltd.
01 1Eperisone Hydrochloride JP
01 1China
Registration Number : 231MF10073
Registrant's Address : No. 2066 Tangkou Road, Economy and Technology Development Zone, Hefei, Anhui Province...
Initial Date of Registration : 2019-03-15
Latest Date of Registration : 2023-01-25
A Eperisone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eperisone Hydrochloride, including repackagers and relabelers. The FDA regulates Eperisone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eperisone Hydrochloride 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 Eperisone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eperisone Hydrochloride supplier is an individual or a company that provides Eperisone Hydrochloride active pharmaceutical ingredient (API) or Eperisone Hydrochloride finished formulations upon request. The Eperisone Hydrochloride suppliers may include Eperisone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Eperisone Hydrochloride 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 Eperisone Hydrochloride Drug Master File in Japan (Eperisone Hydrochloride JDMF) empowers Eperisone Hydrochloride 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 Eperisone Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Eperisone Hydrochloride 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 Eperisone Hydrochloride suppliers with JDMF on PharmaCompass.
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