01 1Alps Pharmaceutical Co., Ltd.
01 1Magnesium L- aspartic acid, potassium
01 1Japan
Magnesium and potassium L-aspartate
Registration Number : 217MF11042
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2005-12-02
Latest Date of Registration : 2009-07-30
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PharmaCompass offers a list of Magnesium Aspartate 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 Magnesium Aspartate manufacturer or Magnesium Aspartate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Aspartate manufacturer or Magnesium Aspartate supplier.
PharmaCompass also assists you with knowing the Magnesium Aspartate API Price utilized in the formulation of products. Magnesium Aspartate API Price is not always fixed or binding as the Magnesium Aspartate Price is obtained through a variety of data sources. The Magnesium Aspartate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A L-aspartate potassium and magnesium salt mixture manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-aspartate potassium and magnesium salt mixture, including repackagers and relabelers. The FDA regulates L-aspartate potassium and magnesium salt mixture manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-aspartate potassium and magnesium salt mixture 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 L-aspartate potassium and magnesium salt mixture manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A L-aspartate potassium and magnesium salt mixture supplier is an individual or a company that provides L-aspartate potassium and magnesium salt mixture active pharmaceutical ingredient (API) or L-aspartate potassium and magnesium salt mixture finished formulations upon request. The L-aspartate potassium and magnesium salt mixture suppliers may include L-aspartate potassium and magnesium salt mixture API manufacturers, exporters, distributors and traders.
click here to find a list of L-aspartate potassium and magnesium salt mixture 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 L-aspartate potassium and magnesium salt mixture Drug Master File in Japan (L-aspartate potassium and magnesium salt mixture JDMF) empowers L-aspartate potassium and magnesium salt mixture 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 L-aspartate potassium and magnesium salt mixture JDMF during the approval evaluation for pharmaceutical products. At the time of L-aspartate potassium and magnesium salt mixture 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 L-aspartate potassium and magnesium salt mixture suppliers with JDMF on PharmaCompass.
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