01 2Komatsuya Co., Ltd.
02 1Kyongbo Pharmaceutical Co. , Ltd.
03 1Showa Chemical Co., Ltd.
01 1Day stations mosapride acid hydrate (production only)
02 1Japanese Pharmaceutical Codex sodium ferrous citrate
03 2Japanese Pharmacopoeia sodium citrate hydrate
01 3Japan
02 1South Korea
Japanese Pharmacopoeia Standards for Non-Official Drugs: Sodium Ferrous Citrate
Registration Number : 224MF10212
Registrant's Address : Matsuura Sakaisuji Honmachi Building, 1-9-28 Kyutaro-cho, Chuo-ku, Osaka City, Osaka ...
Initial Date of Registration : 2012-10-29
Latest Date of Registration : 2012-10-29
Japanese Pharmacopoeia Sodium Citrate Hydrate
Registration Number : 219MF10179
Registrant's Address : Matsuura Sakaisuji Honmachi Building, 1-9-28 Kyutaro-cho, Chuo-ku, Osaka City, Osaka ...
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2007-06-01
Japanese Pharmacopoeia Mosapride Citrate Hydrate (For Manufacturing Use Only)
Registration Number : 223MF10104
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2011-07-15
Latest Date of Registration : 2011-07-15
Japanese Pharmacopoeia Sodium Citrate Hydrate
Registration Number : 218MF10737
Registrant's Address : 18-23 Yoshino-cho, Suita City, Osaka Prefecture
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2007-09-28
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PharmaCompass offers a list of Citric Acid 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 Citric Acid manufacturer or Citric Acid supplier for your needs.
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A Chemfill manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chemfill, including repackagers and relabelers. The FDA regulates Chemfill manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chemfill 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 Chemfill manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Chemfill supplier is an individual or a company that provides Chemfill active pharmaceutical ingredient (API) or Chemfill finished formulations upon request. The Chemfill suppliers may include Chemfill API manufacturers, exporters, distributors and traders.
click here to find a list of Chemfill 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 Chemfill Drug Master File in Japan (Chemfill JDMF) empowers Chemfill 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 Chemfill JDMF during the approval evaluation for pharmaceutical products. At the time of Chemfill 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 Chemfill suppliers with JDMF on PharmaCompass.
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