01 6Active Pharma Inc.
02 1DNP Fine Chemicals Utsunomiya Co., Ltd.
03 1ESHYASI PHARMA LIMITED
04 1JEIL PHARMACEUTICAL CO. , LTD.
05 1Korea Biochem Pharm. Inc.
06 1Ohara Pharmaceutical Co., Ltd.
07 1Sanyo Chemical Research Institute Co., Ltd.
01 1Salpogrelate hydrochloride
02 1Salpogrelate hydrochloride P
03 1Salpogrelate hydrochloride T
04 8Sarpogrelate hydrochloride
05 1Sarpogrelate hydrochloride P
01 1Gabon
02 1India
03 8Japan
04 2South Korea
Registration Number : 228MF10193
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2016-10-05
Latest Date of Registration : 2016-10-05
Registration Number : 301MF10004
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2019-05-15
Latest Date of Registration : 2019-05-15
Registration Number : 230MF10062
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2018-05-08
Latest Date of Registration : 2018-05-08
Registration Number : 227MF10170
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2015-06-18
Latest Date of Registration : 2015-06-18
Registration Number : 220MF10185
Registrant's Address : 1062-8 Honjo, Nishikata-cho, Tochigi City, Tochigi Prefecture
Initial Date of Registration : 2008-07-31
Latest Date of Registration : 2012-09-21
Registration Number : 225MF10228
Registrant's Address : Plot No. :B-7/31, 32, 33. Krishna Industrial Estate, Opp. BIDC, Gorwa, Baroda-390 016...
Initial Date of Registration : 2013-12-18
Latest Date of Registration : 2013-12-18
Registration Number : 228MF10104
Registrant's Address : 343, Sapyeong-daero, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2016-06-06
Latest Date of Registration : 2016-06-06
Registration Number : 231MF10008
Registrant's Address : #204, Sandan-gil, Jeonui-myeon, Sejong, Korea
Initial Date of Registration : 2019-01-10
Latest Date of Registration : 2019-01-10
Registration Number : 221MF10040
Registrant's Address : 121-15 Toriiino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2009-02-23
Latest Date of Registration : 2009-02-23
Registration Number : 223MF10071
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2011-05-27
Latest Date of Registration : 2011-05-27
A Sarpogrelate Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sarpogrelate Hydrochloride, including repackagers and relabelers. The FDA regulates Sarpogrelate Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sarpogrelate Hydrochloride 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 Sarpogrelate Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sarpogrelate Hydrochloride supplier is an individual or a company that provides Sarpogrelate Hydrochloride active pharmaceutical ingredient (API) or Sarpogrelate Hydrochloride finished formulations upon request. The Sarpogrelate Hydrochloride suppliers may include Sarpogrelate Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Sarpogrelate Hydrochloride 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 Sarpogrelate Hydrochloride Drug Master File in Japan (Sarpogrelate Hydrochloride JDMF) empowers Sarpogrelate Hydrochloride 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 Sarpogrelate Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Sarpogrelate Hydrochloride 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 Sarpogrelate Hydrochloride suppliers with JDMF on PharmaCompass.
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