01 1Taihei Chemical Industry Co., Ltd.
01 1Japan Pharmaceutical Codex dihydrogen phosphate potassium (production only)
01 1Japan
Japanese Pharmacopoeia Non-Drug Standard Dipotassium Phosphate (For manufacturing only)
Registration Number : 221MF10233
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Higashi-Koraibashi 1-16
Initial Date of Registration : 2009-10-26
Latest Date of Registration : 2016-09-02
89
PharmaCompass offers a list of Monosodium 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 Monosodium Phosphate manufacturer or Monosodium Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Monosodium Phosphate manufacturer or Monosodium Phosphate supplier.
PharmaCompass also assists you with knowing the Monosodium Phosphate API Price utilized in the formulation of products. Monosodium Phosphate API Price is not always fixed or binding as the Monosodium Phosphate Price is obtained through a variety of data sources. The Monosodium Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E339 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E339, including repackagers and relabelers. The FDA regulates E339 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E339 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 E339 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E339 supplier is an individual or a company that provides E339 active pharmaceutical ingredient (API) or E339 finished formulations upon request. The E339 suppliers may include E339 API manufacturers, exporters, distributors and traders.
click here to find a list of E339 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 E339 Drug Master File in Japan (E339 JDMF) empowers E339 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 E339 JDMF during the approval evaluation for pharmaceutical products. At the time of E339 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 E339 suppliers with JDMF on PharmaCompass.
We have 1 companies offering E339
Get in contact with the supplier of your choice:
