01 1Cambrex Profarmaco Milano S. r. l.
02 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 2Chlordiazepoxide
01 1Italy
02 1U.S.A
Registration Number : 218MF10145
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2009-07-21
Registration Number : 222MF10163
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2010-06-02
Latest Date of Registration : 2010-06-02
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PharmaCompass offers a list of Chlordiazepoxide 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 Chlordiazepoxide manufacturer or Chlordiazepoxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlordiazepoxide manufacturer or Chlordiazepoxide supplier.
PharmaCompass also assists you with knowing the Chlordiazepoxide API Price utilized in the formulation of products. Chlordiazepoxide API Price is not always fixed or binding as the Chlordiazepoxide Price is obtained through a variety of data sources. The Chlordiazepoxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zetran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zetran, including repackagers and relabelers. The FDA regulates Zetran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zetran 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 Zetran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zetran supplier is an individual or a company that provides Zetran active pharmaceutical ingredient (API) or Zetran finished formulations upon request. The Zetran suppliers may include Zetran API manufacturers, exporters, distributors and traders.
click here to find a list of Zetran 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 Zetran Drug Master File in Japan (Zetran JDMF) empowers Zetran 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 Zetran JDMF during the approval evaluation for pharmaceutical products. At the time of Zetran 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 Zetran suppliers with JDMF on PharmaCompass.
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