01 1Cambrex Profarmaco Milano S. r. l.
01 1Clorazepate dipotassium
01 1U.S.A
Registration Number : 219MF10063
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2019-08-29
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PharmaCompass offers a list of Clorazepate Dipotassium 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 Clorazepate Dipotassium manufacturer or Clorazepate Dipotassium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clorazepate Dipotassium manufacturer or Clorazepate Dipotassium supplier.
PharmaCompass also assists you with knowing the Clorazepate Dipotassium API Price utilized in the formulation of products. Clorazepate Dipotassium API Price is not always fixed or binding as the Clorazepate Dipotassium Price is obtained through a variety of data sources. The Clorazepate Dipotassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tranxene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tranxene, including repackagers and relabelers. The FDA regulates Tranxene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tranxene 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 Tranxene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tranxene supplier is an individual or a company that provides Tranxene active pharmaceutical ingredient (API) or Tranxene finished formulations upon request. The Tranxene suppliers may include Tranxene API manufacturers, exporters, distributors and traders.
click here to find a list of Tranxene 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 Tranxene Drug Master File in Japan (Tranxene JDMF) empowers Tranxene 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 Tranxene JDMF during the approval evaluation for pharmaceutical products. At the time of Tranxene 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 Tranxene suppliers with JDMF on PharmaCompass.
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