Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 2PCAS
02 1Siegfried Evionnaz SA
01 2Oxybutynin hydrochloride
02 1Oxybutynin hydrochloride Oxybutynin Hydrochloride
01 2France
02 1Switzerland
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 226MF10078
Registrant's Address : 21 chemin de la Sauvegarde, 21 Ecully Parc CS 33167 69134 Ecully Cedex FRANCE
Initial Date of Registration : 2014-04-02
Latest Date of Registration : 2018-09-21
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF10148
Registrant's Address : 23, rue Bossuet Z. I. de la Vigne aux Loups F-91160 LONGJUMEAU France
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2008-11-17
Registration Number : 221MF10114
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2009-06-10
Latest Date of Registration : 2009-06-10
A Oxybutynin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxybutynin Hydrochloride, including repackagers and relabelers. The FDA regulates Oxybutynin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxybutynin Hydrochloride 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 Oxybutynin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxybutynin Hydrochloride supplier is an individual or a company that provides Oxybutynin Hydrochloride active pharmaceutical ingredient (API) or Oxybutynin Hydrochloride finished formulations upon request. The Oxybutynin Hydrochloride suppliers may include Oxybutynin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Oxybutynin Hydrochloride 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 Oxybutynin Hydrochloride Drug Master File in Japan (Oxybutynin Hydrochloride JDMF) empowers Oxybutynin Hydrochloride 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 Oxybutynin Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Oxybutynin Hydrochloride 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 Oxybutynin Hydrochloride suppliers with JDMF on PharmaCompass.
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