01 1Taihei Chemical Industry Co., Ltd.
01 1Japanese Pharmaceutical Codex potassium dihydrogen phosphate (manufactured only)
01 1Japan
Japanese Pharmacopoeia Non-Drug Standard Potassium Dihydrogen Phosphate (For manufacturing only)
Registration Number : 218MF10726
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Higashi-Koraibashi 1-16
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2006-09-06
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PharmaCompass offers a list of Potassium Dihydrogen Phosphate 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 Potassium Dihydrogen Phosphate manufacturer or Potassium Dihydrogen Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Potassium Dihydrogen Phosphate manufacturer or Potassium Dihydrogen Phosphate supplier.
PharmaCompass also assists you with knowing the Potassium Dihydrogen Phosphate API Price utilized in the formulation of products. Potassium Dihydrogen Phosphate API Price is not always fixed or binding as the Potassium Dihydrogen Phosphate Price is obtained through a variety of data sources. The Potassium Dihydrogen Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Potassium orthophosphate, dihydrogen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Potassium orthophosphate, dihydrogen, including repackagers and relabelers. The FDA regulates Potassium orthophosphate, dihydrogen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Potassium orthophosphate, dihydrogen 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 Potassium orthophosphate, dihydrogen supplier is an individual or a company that provides Potassium orthophosphate, dihydrogen active pharmaceutical ingredient (API) or Potassium orthophosphate, dihydrogen finished formulations upon request. The Potassium orthophosphate, dihydrogen suppliers may include Potassium orthophosphate, dihydrogen API manufacturers, exporters, distributors and traders.
click here to find a list of Potassium orthophosphate, dihydrogen 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 Potassium orthophosphate, dihydrogen Drug Master File in Japan (Potassium orthophosphate, dihydrogen JDMF) empowers Potassium orthophosphate, dihydrogen 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 Potassium orthophosphate, dihydrogen JDMF during the approval evaluation for pharmaceutical products. At the time of Potassium orthophosphate, dihydrogen 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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