01 2Active Pharma Inc.
02 1INIST ST CO. , LTD.
03 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
04 1Sanyo Chemical Research Institute Co., Ltd.
05 1Shandong New Time Pharmaceutical Co. , Ltd.
06 1Tokuyama Corporation
07 2Yoshindo Co., Ltd.
01 1Japanese Pharmacopoeia mosapride acid hydrate production-only
02 6Mosapride acid hydrate
03 1Mosapride citrate hydrate (N)
04 1Mosapride citrate hydrate T
01 1China
02 1Gabon
03 6Japan
04 1South Korea
Registration Number : 228MF10229
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2016-12-14
Latest Date of Registration : 2016-12-14
Registration Number : 225MF10151
Registrant's Address : 500, Sinnae-ro, Geumwang-eup, Eumseong-gun, Chungcheongbuk-do, Korea
Initial Date of Registration : 2013-08-09
Latest Date of Registration : 2013-08-09
Registration Number : 304MF10119
Registrant's Address : No. 1, North Outer Ring Road, Feixian County, Shandong Province, China
Initial Date of Registration : 2022-08-10
Latest Date of Registration : 2024-04-18
Japanese Pharmacopoeia Mosapride Citrate Hydrate For manufacturing only
Registration Number : 223MF10097
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2011-07-06
Latest Date of Registration : 2011-07-06
Registration Number : 223MF10100
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2011-07-11
Latest Date of Registration : 2011-07-11
Registration Number : 223MF10077
Registrant's Address : 1-1 Mikage-cho, Shunan City, Yamaguchi Prefecture
Initial Date of Registration : 2011-06-07
Latest Date of Registration : 2011-06-07
Registration Number : 223MF10068
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2011-05-25
Latest Date of Registration : 2011-05-25
Registration Number : 223MF10066
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2011-05-18
Latest Date of Registration : 2011-05-18
Registration Number : 230MF10108
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2018-08-08
Latest Date of Registration : 2020-06-16
A Mosapride Citrate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mosapride Citrate Dihydrate, including repackagers and relabelers. The FDA regulates Mosapride Citrate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mosapride Citrate Dihydrate 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 Mosapride Citrate Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mosapride Citrate Dihydrate supplier is an individual or a company that provides Mosapride Citrate Dihydrate active pharmaceutical ingredient (API) or Mosapride Citrate Dihydrate finished formulations upon request. The Mosapride Citrate Dihydrate suppliers may include Mosapride Citrate Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Mosapride Citrate Dihydrate 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 Mosapride Citrate Dihydrate Drug Master File in Japan (Mosapride Citrate Dihydrate JDMF) empowers Mosapride Citrate Dihydrate 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 Mosapride Citrate Dihydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Mosapride Citrate Dihydrate 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 Mosapride Citrate Dihydrate suppliers with JDMF on PharmaCompass.
We have 7 companies offering Mosapride Citrate Dihydrate
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