01 2Maruzen Pharmaceuticals Co., Ltd.
01 1Monoammonium Glycyrrhizinate
02 1Monoammonium glycyrrhizinate
01 2Japan
Registration Number : 303MF10177
Registrant's Address : 14703-10 Mukaihigashicho, Onomichi City, Hiroshima Prefecture
Initial Date of Registration : 2021-12-09
Latest Date of Registration : 2021-12-09
Registration Number : 222MF10017
Registrant's Address : 14703-10 Mukaihigashicho, Onomichi City, Hiroshima Prefecture
Initial Date of Registration : 2010-01-07
Latest Date of Registration : 2010-01-07
A Ammonium Glycyrrhizinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ammonium Glycyrrhizinate, including repackagers and relabelers. The FDA regulates Ammonium Glycyrrhizinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ammonium Glycyrrhizinate 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 Ammonium Glycyrrhizinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ammonium Glycyrrhizinate supplier is an individual or a company that provides Ammonium Glycyrrhizinate active pharmaceutical ingredient (API) or Ammonium Glycyrrhizinate finished formulations upon request. The Ammonium Glycyrrhizinate suppliers may include Ammonium Glycyrrhizinate API manufacturers, exporters, distributors and traders.
click here to find a list of Ammonium Glycyrrhizinate 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 Ammonium Glycyrrhizinate Drug Master File in Japan (Ammonium Glycyrrhizinate JDMF) empowers Ammonium Glycyrrhizinate 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 Ammonium Glycyrrhizinate JDMF during the approval evaluation for pharmaceutical products. At the time of Ammonium Glycyrrhizinate 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 Ammonium Glycyrrhizinate suppliers with JDMF on PharmaCompass.
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