01 1BEC Chemicals Pvt. Ltd
02 1BIDACHEM S. p. A.
03 2DONGBANG FUTURE TECH & LIFE CO. , LTD.
04 1EUROAPI Germany GmbH
05 2HUBEI XUNDA PHARMACEUTICAL CO. , LTD.
06 1HUBEI XUNDA PHARMACEUTICAL CO. ,LTD
07 1Hamari PFST Co., Ltd.
08 1KOLON LIFE SCIENCE, INC.
09 1Sogo Pharmaceutical Co., Ltd.
10 1Southwest Synthetic Pharmaceutical Corp. , Ltd.
11 1YUHAN CORPORATION
12 1Zhejiang Raybow Pharmaceutical Co. , Ltd.
01 1Japanese Pharmacopoeia ketoprofen
02 4Japanese Pharmacopoeia ketoprofen (production only)
03 1KETOPROFEN
04 8Ketoprofen
01 5China
02 1Gabon
03 1India
04 1Italy
05 1Japan
06 4South Korea
07 1U.S.A
Registration Number : 228MF10058
Registrant's Address : S-86, IBI House, Chimatpada, Marol Naka, Andheri Kurla Road, India-400 059 Mumbai, Ma...
Initial Date of Registration : 2016-02-18
Latest Date of Registration : 2016-02-18
Registration Number : 226MF10042
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2014-02-19
Latest Date of Registration : 2014-02-19
Registration Number : 229MF10068
Registrant's Address : No. 2, JINPAN ROAD, WUXUE, HUBEI PROVINCE, CHINA
Initial Date of Registration : 2017-03-22
Latest Date of Registration : 2017-03-22
Registration Number : 226MF10159
Registrant's Address : NO. 117, EAST-YONGNING ROAD, WUXUE, HUBEI, CHINA
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2014-09-01
Registration Number : 227MF10278
Registrant's Address : No. 2, JINPAN ROAD, WUXUE, HUBEI PROVINCE, CHINA
Initial Date of Registration : 2015-12-11
Latest Date of Registration : 2015-12-11
Japanese Pharmacopoeia Ketoprofen
Registration Number : 218MF10023
Registrant's Address : 13, KOLON-RO, GWACHEON-SI, GYEONGGI-DO, KOREA
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2007-01-10
Registration Number : 217MF10425
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-08-19
Latest Date of Registration : 2007-07-06
Registration Number : 222MF10169
Registrant's Address : Brueningstrasse 50, 65926 Frankfurt am Main, Germany
Initial Date of Registration : 2010-06-08
Latest Date of Registration : 2022-06-15
Registration Number : 217MF10546
Registrant's Address : 49-6, DAEBANG-DONG, DONGJAK-GU, SEOUL, KOREA
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-11-05
Japanese Pharmacopoeia Ketoprofen (for manufacturing only)
Registration Number : 225MF10157
Registrant's Address : 18 Nan Yang San Road, Lin Hai City, Taizhou City Zhejiang Province
Initial Date of Registration : 2013-08-14
Latest Date of Registration : 2013-08-14
A Ketoprofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ketoprofen, including repackagers and relabelers. The FDA regulates Ketoprofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ketoprofen 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 Ketoprofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ketoprofen supplier is an individual or a company that provides Ketoprofen active pharmaceutical ingredient (API) or Ketoprofen finished formulations upon request. The Ketoprofen suppliers may include Ketoprofen API manufacturers, exporters, distributors and traders.
click here to find a list of Ketoprofen 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 Ketoprofen Drug Master File in Japan (Ketoprofen JDMF) empowers Ketoprofen 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 Ketoprofen JDMF during the approval evaluation for pharmaceutical products. At the time of Ketoprofen 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 Ketoprofen suppliers with JDMF on PharmaCompass.
We have 10 companies offering Ketoprofen
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