01 4Fuji Chemical Industry Co., Ltd.
01 1Magnesium aluminometasilicate (FH1) (production only)
02 1Magnesium aluminometasilicate (S1) (production only)
03 1Magnesium aluminometasilicate (S2) (production only)
04 1Undried magnesium aluminometasilicate
01 4Japan
Wet Magnesium Aluminometasilicate
Registration Number : 218MF10858
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2006-11-06
Latest Date of Registration : 2006-11-06
Magnesium aluminometasilicate (S1) (for manufacturing only)
Registration Number : 221MF10096
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2009-05-13
Latest Date of Registration : 2009-05-13
Magnesium aluminometasilicate (FH1) (for manufacturing only)
Registration Number : 221MF10095
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2009-05-13
Latest Date of Registration : 2009-05-13
Magnesium aluminometasilicate (S2) (for manufacturing only)
Registration Number : 221MF10093
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2009-05-13
Latest Date of Registration : 2009-05-13
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PharmaCompass offers a list of Aluminum Magnesium Silicate 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 Aluminum Magnesium Silicate manufacturer or Aluminum Magnesium Silicate supplier for your needs.
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PharmaCompass also assists you with knowing the Aluminum Magnesium Silicate API Price utilized in the formulation of products. Aluminum Magnesium Silicate API Price is not always fixed or binding as the Aluminum Magnesium Silicate Price is obtained through a variety of data sources. The Aluminum Magnesium Silicate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neusilin US2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neusilin US2, including repackagers and relabelers. The FDA regulates Neusilin US2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neusilin US2 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Neusilin US2 supplier is an individual or a company that provides Neusilin US2 active pharmaceutical ingredient (API) or Neusilin US2 finished formulations upon request. The Neusilin US2 suppliers may include Neusilin US2 API manufacturers, exporters, distributors and traders.
click here to find a list of Neusilin US2 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 Neusilin US2 Drug Master File in Japan (Neusilin US2 JDMF) empowers Neusilin US2 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 Neusilin US2 JDMF during the approval evaluation for pharmaceutical products. At the time of Neusilin US2 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 Neusilin US2 suppliers with JDMF on PharmaCompass.
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