01 2Kyowa Chemical Industry Co., Ltd.
01 2Japanese Pharmacopoeia magnesium carbonate (production only)
01 2Japan
Japanese Pharmacopoeia Magnesium Carbonate (for manufacturing purposes 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 : 2025-04-08
Japanese Pharmacopoeia Magnesium Carbonate (for manufacturing purposes 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 : 2024-12-25
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PharmaCompass offers a list of Magnesium Carbonate 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 Carbonate manufacturer or Magnesium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Carbonate manufacturer or Magnesium Carbonate supplier.
PharmaCompass also assists you with knowing the Magnesium Carbonate API Price utilized in the formulation of products. Magnesium Carbonate API Price is not always fixed or binding as the Magnesium Carbonate Price is obtained through a variety of data sources. The Magnesium Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DTXSID4049660 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DTXSID4049660, including repackagers and relabelers. The FDA regulates DTXSID4049660 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DTXSID4049660 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 DTXSID4049660 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DTXSID4049660 supplier is an individual or a company that provides DTXSID4049660 active pharmaceutical ingredient (API) or DTXSID4049660 finished formulations upon request. The DTXSID4049660 suppliers may include DTXSID4049660 API manufacturers, exporters, distributors and traders.
click here to find a list of DTXSID4049660 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 DTXSID4049660 Drug Master File in Japan (DTXSID4049660 JDMF) empowers DTXSID4049660 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 DTXSID4049660 JDMF during the approval evaluation for pharmaceutical products. At the time of DTXSID4049660 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 DTXSID4049660 suppliers with JDMF on PharmaCompass.
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