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
A Dexibuprofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexibuprofen, including repackagers and relabelers. The FDA regulates Dexibuprofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexibuprofen 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 Dexibuprofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dexibuprofen supplier is an individual or a company that provides Dexibuprofen active pharmaceutical ingredient (API) or Dexibuprofen finished formulations upon request. The Dexibuprofen suppliers may include Dexibuprofen API manufacturers, exporters, distributors and traders.
click here to find a list of Dexibuprofen 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 Dexibuprofen Drug Master File in Japan (Dexibuprofen JDMF) empowers Dexibuprofen 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 Dexibuprofen JDMF during the approval evaluation for pharmaceutical products. At the time of Dexibuprofen 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 Dexibuprofen suppliers with JDMF on PharmaCompass.
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