01 1Sandoz GmbH
01 1Crude Cefozopran
01 1Switzerland
Registration Number : 218MF10354
Registrant's Address : Biochemiesstrasse 10,6250 Kundl, Austria
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2006-03-17
A Cefozopran Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefozopran Hydrochloride, including repackagers and relabelers. The FDA regulates Cefozopran Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefozopran 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.
A Cefozopran Hydrochloride supplier is an individual or a company that provides Cefozopran Hydrochloride active pharmaceutical ingredient (API) or Cefozopran Hydrochloride finished formulations upon request. The Cefozopran Hydrochloride suppliers may include Cefozopran Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cefozopran 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 Cefozopran Hydrochloride Drug Master File in Japan (Cefozopran Hydrochloride JDMF) empowers Cefozopran 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 Cefozopran Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Cefozopran 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 Cefozopran Hydrochloride suppliers with JDMF on PharmaCompass.
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