01 1Daito Co., Ltd.
02 2FDC LIMITED.
03 1GMFC LABS PVT LTD
04 1Hy-Gro Chemicals Pharmatek Private Limited.
05 1Hy-Gro Chemicals Pharmtek Private Limited
06 3KOLON LIFE SCIENCE, INC.
07 1Lee Pharma Limited
08 1PHARMARON MANUFACTURING SERVICES (UK) LTD.
01 1Day stations flurbiprofen (production only)
02 1FLURBIPROFEN
03 4Flurbiprofen
04 1Flurbiprofen (C)
05 1Flurbiprofen (N)
06 1Japanese Pharmacopoeia flurbiprofen
07 1Japanese Pharmacopoeia flurbiprofen (production only)
08 1S-Flurbiprofen
01 1China
02 5India
03 1Japan
04 3South Korea
05 1United Kingdom
Registration Number : 217MF11168
Registrant's Address : Windmill Industrial Estate, Shotton Lane, Cramlington, Northumberland NE23 3JL, Unite...
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2016-05-09
JP Flurbiprofen (for manufacturing only)
Registration Number : 217MF10636
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-09-29
Latest Date of Registration : 2007-07-02
Registration Number : 219MF10187
Registrant's Address : 142-48,s,v,road,jogeshwari(w),mumbai-400 102 India
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2007-06-01
Japanese Pharmacopoeia Flurbiprofen (for manufacturing only)
Registration Number : 218MF10559
Registrant's Address : 142-48, s. v. road, jogeshwari(w), mumbai-400 102 India
Initial Date of Registration : 2006-06-02
Latest Date of Registration : 2007-05-15
Registration Number : 305MF10073
Registrant's Address : Plot No. 113, ISTA Homes, 4th Floor, Kavuri Hills Road, CBI Colony, Jubilee Hills, Hy...
Initial Date of Registration : 2023-06-14
Latest Date of Registration : 2023-06-14
Registration Number : 306MF10037
Registrant's Address : Unit No. 203 & 204, 2nd Floor, Ashoka Bhoopal Chambers, Sardar Patel Road, Secunderab...
Initial Date of Registration : 2024-03-06
Latest Date of Registration : 2024-03-06
Registration Number : 222MF10162
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2010-06-02
Latest Date of Registration : 2010-06-02
Registration Number : 303MF10078
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2021-05-13
Latest Date of Registration : 2021-05-13
Registration Number : 306MF10014
Registrant's Address : SY. No. :257 & 258/1, Door No.: 11-6/56-C, Opp: IDPL Factory, Moosapet, Balanagar (Po...
Initial Date of Registration : 2024-01-24
Latest Date of Registration : 2024-01-24
Registration Number : 306MF10033
Registrant's Address : Unit No. 203 & 204, 2nd Floor, Ashoka Bhoopal Chambers, Sardar Patel Road, Secunderab...
Initial Date of Registration : 2024-02-29
Latest Date of Registration : 2024-02-29
A Flurbiprofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flurbiprofen, including repackagers and relabelers. The FDA regulates Flurbiprofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flurbiprofen 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 Flurbiprofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flurbiprofen supplier is an individual or a company that provides Flurbiprofen active pharmaceutical ingredient (API) or Flurbiprofen finished formulations upon request. The Flurbiprofen suppliers may include Flurbiprofen API manufacturers, exporters, distributors and traders.
click here to find a list of Flurbiprofen 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 Flurbiprofen Drug Master File in Japan (Flurbiprofen JDMF) empowers Flurbiprofen 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 Flurbiprofen JDMF during the approval evaluation for pharmaceutical products. At the time of Flurbiprofen 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 Flurbiprofen suppliers with JDMF on PharmaCompass.
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