01 1Taihei Chemical Industry Co., Ltd.
01 1Japan Pharmaceutical Codex dihydrogen phosphate potassium (production only)
01 1Japan
Registration Number : 221MF10233
Registrant's Address : 1-16 Higashi-Koraibashi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2009-10-26
Latest Date of Registration : 2016-09-02
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PharmaCompass offers a list of Monosodium Phosphate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Monosodium Phosphate manufacturer or Monosodium Phosphate supplier for your needs.
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A Monosodium monophosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monosodium monophosphate, including repackagers and relabelers. The FDA regulates Monosodium monophosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monosodium monophosphate 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 Monosodium monophosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Monosodium monophosphate supplier is an individual or a company that provides Monosodium monophosphate active pharmaceutical ingredient (API) or Monosodium monophosphate finished formulations upon request. The Monosodium monophosphate suppliers may include Monosodium monophosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Monosodium monophosphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Monosodium monophosphate Drug Master File in Japan (Monosodium monophosphate JDMF) empowers Monosodium monophosphate 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 Monosodium monophosphate JDMF during the approval evaluation for pharmaceutical products. At the time of Monosodium monophosphate 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 Monosodium monophosphate suppliers with JDMF on PharmaCompass.
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