Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak a. s.
01 1Hydrochloric acid dosulepin
01 1Czech Republic
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registration Number : 219MF10153
Registrant's Address : Na Vlcinci 16/3 771 17 Olomouc Czech republic
Initial Date of Registration : 2007-04-27
Latest Date of Registration : 2007-04-27
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PharmaCompass offers a list of Dosulepin HCl 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 Dosulepin HCl manufacturer or Dosulepin HCl supplier for your needs.
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PharmaCompass also assists you with knowing the Dosulepin HCl API Price utilized in the formulation of products. Dosulepin HCl API Price is not always fixed or binding as the Dosulepin HCl Price is obtained through a variety of data sources. The Dosulepin HCl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dothiepin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dothiepin, including repackagers and relabelers. The FDA regulates Dothiepin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dothiepin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Dothiepin supplier is an individual or a company that provides Dothiepin active pharmaceutical ingredient (API) or Dothiepin finished formulations upon request. The Dothiepin suppliers may include Dothiepin API manufacturers, exporters, distributors and traders.
click here to find a list of Dothiepin 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 Dothiepin Drug Master File in Japan (Dothiepin JDMF) empowers Dothiepin 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 Dothiepin JDMF during the approval evaluation for pharmaceutical products. At the time of Dothiepin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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