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 HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chloroprocaine HCl, including repackagers and relabelers. The FDA regulates Chloroprocaine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chloroprocaine HCl 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 HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chloroprocaine HCl supplier is an individual or a company that provides Chloroprocaine HCl active pharmaceutical ingredient (API) or Chloroprocaine HCl finished formulations upon request. The Chloroprocaine HCl suppliers may include Chloroprocaine HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Chloroprocaine HCl 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 HCl Drug Master File in Japan (Chloroprocaine HCl JDMF) empowers Chloroprocaine HCl 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 HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Chloroprocaine HCl 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 HCl suppliers with JDMF on PharmaCompass.
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