01 1Cambrex Profarmaco Milano S. r. l.
02 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 2Lorazepam
01 1Italy
02 1U.S.A
Registration Number : 218MF10781
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-09-22
Latest Date of Registration : 2020-11-26
Registration Number : 217MF10849
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2009-04-14
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PharmaCompass offers a list of Lorazepam API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Lorazepam manufacturer or Lorazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lorazepam manufacturer or Lorazepam supplier.
A Bonton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bonton, including repackagers and relabelers. The FDA regulates Bonton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bonton 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 Bonton manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Bonton supplier is an individual or a company that provides Bonton active pharmaceutical ingredient (API) or Bonton finished formulations upon request. The Bonton suppliers may include Bonton API manufacturers, exporters, distributors and traders.
click here to find a list of Bonton suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Bonton Drug Master File in Japan (Bonton JDMF) empowers Bonton 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 Bonton JDMF during the approval evaluation for pharmaceutical products. At the time of Bonton 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 Bonton suppliers with JDMF on PharmaCompass.
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