01 1Excella GmbH & Co. K.G.
02 1Valdepharm
01 1Trazodone Hydrochloride
02 1Trazodone hydrochloride
01 2Luxembourg
Registration Number : 222MF10059
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2010-02-17
Latest Date of Registration : 2023-11-15
Registration Number : 302MF10058
Registrant's Address : Parc Industriel d'Incarville Parc de la Fringale CS 10606 27106 Val de Reuil Cedex Fr...
Initial Date of Registration : 2020-05-19
Latest Date of Registration : 2020-05-19
A Trazodone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trazodone Hydrochloride, including repackagers and relabelers. The FDA regulates Trazodone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trazodone 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 Trazodone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trazodone Hydrochloride supplier is an individual or a company that provides Trazodone Hydrochloride active pharmaceutical ingredient (API) or Trazodone Hydrochloride finished formulations upon request. The Trazodone Hydrochloride suppliers may include Trazodone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Trazodone 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 Trazodone Hydrochloride Drug Master File in Japan (Trazodone Hydrochloride JDMF) empowers Trazodone 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 Trazodone Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Trazodone 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 Trazodone Hydrochloride suppliers with JDMF on PharmaCompass.
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