01 1Muromachi Chemical Co., Ltd.
01 1Histamine Dihydrochloride
01 1Japan
Registration Number : 231MF10070
Registrant's Address : 1-38-5 Shinshotachicho, Omuta City, Fukuoka Prefecture
Initial Date of Registration : 2019-03-12
Latest Date of Registration : 2020-01-10
A Histamine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histamine Dihydrochloride, including repackagers and relabelers. The FDA regulates Histamine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histamine Dihydrochloride 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 Histamine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histamine Dihydrochloride supplier is an individual or a company that provides Histamine Dihydrochloride active pharmaceutical ingredient (API) or Histamine Dihydrochloride finished formulations upon request. The Histamine Dihydrochloride suppliers may include Histamine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Histamine Dihydrochloride 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 Histamine Dihydrochloride Drug Master File in Japan (Histamine Dihydrochloride JDMF) empowers Histamine Dihydrochloride 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 Histamine Dihydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Histamine Dihydrochloride 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 Histamine Dihydrochloride suppliers with JDMF on PharmaCompass.
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