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, Price,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.
PharmaCompass also assists you with knowing the Lorazepam API Price utilized in the formulation of products. Lorazepam API Price is not always fixed or binding as the Lorazepam Price is obtained through a variety of data sources. The Lorazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lorsilan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lorsilan, including repackagers and relabelers. The FDA regulates Lorsilan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lorsilan 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 Lorsilan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lorsilan supplier is an individual or a company that provides Lorsilan active pharmaceutical ingredient (API) or Lorsilan finished formulations upon request. The Lorsilan suppliers may include Lorsilan API manufacturers, exporters, distributors and traders.
click here to find a list of Lorsilan 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 Lorsilan Drug Master File in Japan (Lorsilan JDMF) empowers Lorsilan 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 Lorsilan JDMF during the approval evaluation for pharmaceutical products. At the time of Lorsilan 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 Lorsilan suppliers with JDMF on PharmaCompass.
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