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