01 1BASF Corporation
02 1SI Group, Inc.
03 1Sogo Pharmaceutical Co., Ltd.
04 1Solara Active Pharma Sciences Limited
01 2Ibuprofen
02 1Ibuprofen Ibuprofen
03 1Ibuprofen pico Nord
01 1Germany
02 1India
03 1Japan
04 1U.S.A
Registration Number : 217MF10984
Registrant's Address : 100 Park Avenue, Florham Park, New Jersey, 07932, United States of America
Initial Date of Registration : 2005-11-21
Latest Date of Registration : 2009-12-18
Registration Number : 223MF10148
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2011-09-30
Latest Date of Registration : 2011-09-30
Registration Number : 220MF10020
Registrant's Address : “Batra Centre”, 28, Sardar Patel Road, Guindy, Chennai-600 032, India
Initial Date of Registration : 2008-01-09
Latest Date of Registration : 2017-02-15
Registration Number : 219MF10324
Registrant's Address : 1790 Hughes Landing Blvd Suite 600, The Woodlands, TX 77380 US
Initial Date of Registration : 2007-10-24
Latest Date of Registration : 2012-12-26
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PharmaCompass offers a list of Ibuprofen 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 Ibuprofen manufacturer or Ibuprofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ibuprofen manufacturer or Ibuprofen supplier.
PharmaCompass also assists you with knowing the Ibuprofen API Price utilized in the formulation of products. Ibuprofen API Price is not always fixed or binding as the Ibuprofen Price is obtained through a variety of data sources. The Ibuprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bruflam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bruflam, including repackagers and relabelers. The FDA regulates Bruflam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bruflam 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 Bruflam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bruflam supplier is an individual or a company that provides Bruflam active pharmaceutical ingredient (API) or Bruflam finished formulations upon request. The Bruflam suppliers may include Bruflam API manufacturers, exporters, distributors and traders.
click here to find a list of Bruflam 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 Bruflam Drug Master File in Japan (Bruflam JDMF) empowers Bruflam 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 Bruflam JDMF during the approval evaluation for pharmaceutical products. At the time of Bruflam 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 Bruflam suppliers with JDMF on PharmaCompass.
We have 4 companies offering Bruflam
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