01 2Kouki Co., Ltd.
02 1Qingdao Taidong Pharmaceutical Co., Ltd.
01 1Glycyrrhizinate A
02 1Gurichin
03 1Gurichin T
01 1China
02 2U.S.A
Registration Number : 220MF10180
Registrant's Address : 2 Sanbancho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2008-07-31
Latest Date of Registration : 2008-07-31
Registration Number : 217MF10863
Registrant's Address : 2 Sanbancho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2008-05-08
Registration Number : 222MF10086
Registrant's Address : No. 22, Huahai Road, Chengyang District, Qingdao City (Huanhai Economic Development Z...
Initial Date of Registration : 2010-03-16
Latest Date of Registration : 2024-10-02
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PharmaCompass offers a list of Dipotassium 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 Dipotassium Glycyrrhizinate manufacturer or Dipotassium Glycyrrhizinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dipotassium Glycyrrhizinate manufacturer or Dipotassium Glycyrrhizinate supplier.
PharmaCompass also assists you with knowing the Dipotassium Glycyrrhizinate API Price utilized in the formulation of products. Dipotassium Glycyrrhizinate API Price is not always fixed or binding as the Dipotassium Glycyrrhizinate Price is obtained through a variety of data sources. The Dipotassium Glycyrrhizinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glycyrrhizin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glycyrrhizin, including repackagers and relabelers. The FDA regulates Glycyrrhizin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glycyrrhizin 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 Glycyrrhizin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glycyrrhizin supplier is an individual or a company that provides Glycyrrhizin active pharmaceutical ingredient (API) or Glycyrrhizin finished formulations upon request. The Glycyrrhizin suppliers may include Glycyrrhizin API manufacturers, exporters, distributors and traders.
click here to find a list of Glycyrrhizin 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 Glycyrrhizin Drug Master File in Japan (Glycyrrhizin JDMF) empowers Glycyrrhizin 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 Glycyrrhizin JDMF during the approval evaluation for pharmaceutical products. At the time of Glycyrrhizin 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 Glycyrrhizin suppliers with JDMF on PharmaCompass.
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