01 2Maruzen Pharmaceuticals Co., Ltd.
01 1Monoammonium Glycyrrhizinate
02 1Monoammonium glycyrrhizinate
01 2Japan
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
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
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PharmaCompass offers a list of Monoammonium Glycyrrhizinate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Monoammonium Glycyrrhizinate manufacturer or Monoammonium Glycyrrhizinate supplier for your needs.
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PharmaCompass also assists you with knowing the Monoammonium Glycyrrhizinate API Price utilized in the formulation of products. Monoammonium Glycyrrhizinate API Price is not always fixed or binding as the Monoammonium Glycyrrhizinate Price is obtained through a variety of data sources. The Monoammonium Glycyrrhizinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH], including repackagers and relabelers. The FDA regulates AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] supplier is an individual or a company that provides AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] active pharmaceutical ingredient (API) or AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] finished formulations upon request. The AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] suppliers may include AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] API manufacturers, exporters, distributors and traders.
click here to find a list of AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] 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 GLYCYRRHIZATE [EP MONOGRAPH] Drug Master File in Japan (AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] JDMF) empowers AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] 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 GLYCYRRHIZATE [EP MONOGRAPH] JDMF during the approval evaluation for pharmaceutical products. At the time of AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH] JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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