01 2Kyowa Chemical Industry Co., Ltd.
01 2Japanese Pharmacopoeia magnesium carbonate (production only)
01 2Japan
Japanese Pharmacopoeia Magnesium Carbonate (for manufacturing only)
Registration Number : 221MF10226
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2009-10-19
Latest Date of Registration : 2009-10-19
Japanese Pharmacopoeia Magnesium Carbonate (for manufacturing only)
Registration Number : 221MF10225
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2009-10-19
Latest Date of Registration : 2009-10-19
A Magnesium Carbonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magnesium Carbonate, including repackagers and relabelers. The FDA regulates Magnesium Carbonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magnesium Carbonate 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 Magnesium Carbonate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Magnesium Carbonate supplier is an individual or a company that provides Magnesium Carbonate active pharmaceutical ingredient (API) or Magnesium Carbonate finished formulations upon request. The Magnesium Carbonate suppliers may include Magnesium Carbonate API manufacturers, exporters, distributors and traders.
click here to find a list of Magnesium Carbonate 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 Magnesium Carbonate Drug Master File in Japan (Magnesium Carbonate JDMF) empowers Magnesium Carbonate 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 Magnesium Carbonate JDMF during the approval evaluation for pharmaceutical products. At the time of Magnesium Carbonate 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 Magnesium Carbonate suppliers with JDMF on PharmaCompass.
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