01 3Ace Japan Co., Ltd.
02 4CSPC Ouyi Pharmaceutical Co. , Ltd.
03 1Daiwa Pharmaceutical Industries Co., Ltd.
04 1Kongo Chemical Co., Ltd.
05 1Sogo Pharmaceutical Co., Ltd.
06 2Taicang Pharmaceutical Factory
01 4Indomethacin
02 2Indomethacin (production only)
03 1Japanese Pharmacopoeia drugs indomethacin
04 5Japanese Pharmacopoeia indomethacin
01 6China
02 1India
03 4Japan
04 1U.S.A
Japanese Pharmacopoeia Indomethacin
Registration Number : 227MF10150
Registrant's Address : Yamagata Prefecture Higashine City Higashine City 5850-1
Initial Date of Registration : 2015-06-01
Latest Date of Registration : 2015-06-01
Japanese Pharmacopoeia Indomethacin
Registration Number : 229MF10198
Registrant's Address : Yamagata Prefecture Higashine City Higashine City 5850-1
Initial Date of Registration : 2017-11-09
Latest Date of Registration : 2017-11-09
Japanese Pharmacopoeia Indomethacin
Registration Number : 227MF10013
Registrant's Address : Yamagata Prefecture Higashine City Higashine City 5850-1
Initial Date of Registration : 2015-01-05
Latest Date of Registration : 2022-10-12
Japanese Pharmacopoeia Indomethacin
Registration Number : 227MF10299
Registrant's Address : No. 276 Zhongshan West Road Shijiazhuang China
Initial Date of Registration : 2015-12-28
Latest Date of Registration : 2015-12-28
Indomethacin (for manufacturing only)
Registration Number : 229MF10011
Registrant's Address : No. 88 Yangzi Road, Economic and Technical Development Zone, Shijiazhuang, Hebei, Chi...
Initial Date of Registration : 2017-01-23
Latest Date of Registration : 2017-01-23
Registration Number : 227MF10265
Registrant's Address : No. 88 Yangzi Road, Economic and Technical Development Zone, Shijiazhuang, Hebei, Chi...
Initial Date of Registration : 2015-11-17
Latest Date of Registration : 2015-11-17
Indomethacin (for manufacturing only)
Registration Number : 217MF11201
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2009-03-16
Registration Number : 217MF10424
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-08-19
Latest Date of Registration : 2008-05-13
Japanese Pharmacopoeia Indomethacin
Registration Number : 225MF10079
Registrant's Address : No. 90, Xingang Road (W.), Taicang
Initial Date of Registration : 2013-04-18
Latest Date of Registration : 2020-12-23
Registration Number : 226MF10187
Registrant's Address : No. 90, Xingang Road (W.), Taicang
Initial Date of Registration : 2014-09-30
Latest Date of Registration : 2021-05-24
A Indomethacin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Indomethacin, including repackagers and relabelers. The FDA regulates Indomethacin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Indomethacin 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 Indomethacin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Indomethacin supplier is an individual or a company that provides Indomethacin active pharmaceutical ingredient (API) or Indomethacin finished formulations upon request. The Indomethacin suppliers may include Indomethacin API manufacturers, exporters, distributors and traders.
click here to find a list of Indomethacin 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 Indomethacin Drug Master File in Japan (Indomethacin JDMF) empowers Indomethacin 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 Indomethacin JDMF during the approval evaluation for pharmaceutical products. At the time of Indomethacin 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 Indomethacin suppliers with JDMF on PharmaCompass.
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