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 1PHARMARON MANUFACTURING SERVICES (UK) LTD.
01 1Day stations flurbiprofen (production only)
02 1FLURBIPROFEN
03 3Flurbiprofen
04 1Flurbiprofen (C)
05 1Flurbiprofen (N)
06 1Japanese Pharmacopoeia flurbiprofen
07 1Japanese Pharmacopoeia flurbiprofen (production only)
08 1S-Flurbiprofen
01 1China
02 4India
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 purposes 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 purposes 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
Japanese Pharmacopoeia Flurbiprofen
Registration Number : 218MF10021
Registrant's Address : 13, KOLON-RO, GWACHEON-SI, GYEONGGI-DO, KOREA
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2007-04-27
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 : 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
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PharmaCompass offers a list of Flurbiprofen API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Flurbiprofen manufacturer or Flurbiprofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flurbiprofen manufacturer or Flurbiprofen supplier.
PharmaCompass also assists you with knowing the Flurbiprofen API Price utilized in the formulation of products. Flurbiprofen API Price is not always fixed or binding as the Flurbiprofen Price is obtained through a variety of data sources. The Flurbiprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acustop Cataplasma manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acustop Cataplasma, including repackagers and relabelers. The FDA regulates Acustop Cataplasma manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acustop Cataplasma 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 Acustop Cataplasma manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acustop Cataplasma supplier is an individual or a company that provides Acustop Cataplasma active pharmaceutical ingredient (API) or Acustop Cataplasma finished formulations upon request. The Acustop Cataplasma suppliers may include Acustop Cataplasma API manufacturers, exporters, distributors and traders.
click here to find a list of Acustop Cataplasma 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 Acustop Cataplasma Drug Master File in Japan (Acustop Cataplasma JDMF) empowers Acustop Cataplasma 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 Acustop Cataplasma JDMF during the approval evaluation for pharmaceutical products. At the time of Acustop Cataplasma 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 Acustop Cataplasma suppliers with JDMF on PharmaCompass.
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