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