01 1Amino Chemicals Ltd.
02 1Rolabo Outsourcing,S. L.
01 1Benazepril hydrochloride
02 1Benazepril hydrochloride "KOA"
01 1Malta
02 1Spain
Benazepril hydrochloride "Coa"
Registration Number : 217MF11297
Registrant's Address : MRA050X, INDUSTRIAL ESTATE MARSA MRS 3000 Malta
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2010-01-26
Registration Number : 227MF10089
Registrant's Address : Poligono Industrial Malpica C/J, No. :3-4 50016 Zaragoza, Spain
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2015-03-12
A Benazepril Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benazepril Hydrochloride, including repackagers and relabelers. The FDA regulates Benazepril Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benazepril 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 Benazepril Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benazepril Hydrochloride supplier is an individual or a company that provides Benazepril Hydrochloride active pharmaceutical ingredient (API) or Benazepril Hydrochloride finished formulations upon request. The Benazepril Hydrochloride suppliers may include Benazepril Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Benazepril 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 Benazepril Hydrochloride Drug Master File in Japan (Benazepril Hydrochloride JDMF) empowers Benazepril 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 Benazepril Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Benazepril 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 Benazepril Hydrochloride suppliers with JDMF on PharmaCompass.
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