Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1PCAS
02 1Sumitomo Chemical Co., Ltd.
01 1Japanese Pharmacopoeia mequitazine
02 1Mequitazine
01 1France
02 1Japan
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF10293
Registrant's Address : 21 chemin de la Sauvegarde, 21 Ecully Parc CS 33167 69134 Ecully Cedex FRANCE
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2012-10-29
Japanese Pharmacopoeia Mequitazine
Registration Number : 218MF10270
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2006-02-17
Latest Date of Registration : 2007-04-27
A Mequitazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mequitazine, including repackagers and relabelers. The FDA regulates Mequitazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mequitazine 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 Mequitazine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mequitazine supplier is an individual or a company that provides Mequitazine active pharmaceutical ingredient (API) or Mequitazine finished formulations upon request. The Mequitazine suppliers may include Mequitazine API manufacturers, exporters, distributors and traders.
click here to find a list of Mequitazine 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 Mequitazine Drug Master File in Japan (Mequitazine JDMF) empowers Mequitazine 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 Mequitazine JDMF during the approval evaluation for pharmaceutical products. At the time of Mequitazine 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 Mequitazine suppliers with JDMF on PharmaCompass.
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