01 1Kyowa Pharma Chemical Co., Ltd.
01 1Japanese Pharmacopoeia procaine hydrochloride (production only)
01 1Japan
Japanese Pharmacopoeia Procaine Hydrochloride (for manufacturing only)
Registration Number : 222MF10113
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2010-03-23
Latest Date of Registration : 2010-03-23
A Chloroprocaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chloroprocaine Hydrochloride, including repackagers and relabelers. The FDA regulates Chloroprocaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chloroprocaine 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 Chloroprocaine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chloroprocaine Hydrochloride supplier is an individual or a company that provides Chloroprocaine Hydrochloride active pharmaceutical ingredient (API) or Chloroprocaine Hydrochloride finished formulations upon request. The Chloroprocaine Hydrochloride suppliers may include Chloroprocaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Chloroprocaine 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 Chloroprocaine Hydrochloride Drug Master File in Japan (Chloroprocaine Hydrochloride JDMF) empowers Chloroprocaine 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 Chloroprocaine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Chloroprocaine 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 Chloroprocaine Hydrochloride suppliers with JDMF on PharmaCompass.
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