EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
01 1Levomepromazine hydrochloride
01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 222MF10095
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2010-03-17
Latest Date of Registration : 2012-04-25
A Levomepromazine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levomepromazine Hydrochloride, including repackagers and relabelers. The FDA regulates Levomepromazine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levomepromazine 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 Levomepromazine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levomepromazine Hydrochloride supplier is an individual or a company that provides Levomepromazine Hydrochloride active pharmaceutical ingredient (API) or Levomepromazine Hydrochloride finished formulations upon request. The Levomepromazine Hydrochloride suppliers may include Levomepromazine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Levomepromazine 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 Levomepromazine Hydrochloride Drug Master File in Japan (Levomepromazine Hydrochloride JDMF) empowers Levomepromazine 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 Levomepromazine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Levomepromazine 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 Levomepromazine Hydrochloride suppliers with JDMF on PharmaCompass.
We have 1 companies offering Levomepromazine Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
