01 1Oril Industry
01 1Trimetazidine hydrochloride
01 1France
Registration Number : 222MF10081
Registrant's Address : 13, rue Auguste Desgene (') tais, 76210 Bolbec, FRANCE
Initial Date of Registration : 2010-03-09
Latest Date of Registration : 2010-03-09
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PharmaCompass offers a list of Trimetazidine 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 Trimetazidine manufacturer or Trimetazidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trimetazidine manufacturer or Trimetazidine supplier.
PharmaCompass also assists you with knowing the Trimetazidine API Price utilized in the formulation of products. Trimetazidine API Price is not always fixed or binding as the Trimetazidine Price is obtained through a variety of data sources. The Trimetazidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Adexor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adexor, including repackagers and relabelers. The FDA regulates Adexor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adexor 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 Adexor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Adexor supplier is an individual or a company that provides Adexor active pharmaceutical ingredient (API) or Adexor finished formulations upon request. The Adexor suppliers may include Adexor API manufacturers, exporters, distributors and traders.
click here to find a list of Adexor 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 Adexor Drug Master File in Japan (Adexor JDMF) empowers Adexor 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 Adexor JDMF during the approval evaluation for pharmaceutical products. At the time of Adexor 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 Adexor suppliers with JDMF on PharmaCompass.
