01 1Sun Chemical Co., Ltd.
01 1Procainamide hydrochloride
01 1China
Registration Number : 218MF10970
Registrant's Address : 29-3 Shinmachi, Yashio City, Saitama Prefecture
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2006-12-01
A Procainamide Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Procainamide Hydrochloride, including repackagers and relabelers. The FDA regulates Procainamide Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Procainamide 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 Procainamide Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Procainamide Hydrochloride supplier is an individual or a company that provides Procainamide Hydrochloride active pharmaceutical ingredient (API) or Procainamide Hydrochloride finished formulations upon request. The Procainamide Hydrochloride suppliers may include Procainamide Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Procainamide 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 Procainamide Hydrochloride Drug Master File in Japan (Procainamide Hydrochloride JDMF) empowers Procainamide 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 Procainamide Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Procainamide 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 Procainamide Hydrochloride suppliers with JDMF on PharmaCompass.
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