01 1DSM Nutritional Products Ltd.
01 1Flucytosine
01 1Netherlands
Registration Number : 222MF10042
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2010-02-04
Latest Date of Registration : 2021-12-22
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PharmaCompass offers a list of Fluocytosine 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 Fluocytosine manufacturer or Fluocytosine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluocytosine manufacturer or Fluocytosine supplier.
PharmaCompass also assists you with knowing the Fluocytosine API Price utilized in the formulation of products. Fluocytosine API Price is not always fixed or binding as the Fluocytosine Price is obtained through a variety of data sources. The Fluocytosine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ancotil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ancotil, including repackagers and relabelers. The FDA regulates Ancotil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ancotil 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 Ancotil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ancotil supplier is an individual or a company that provides Ancotil active pharmaceutical ingredient (API) or Ancotil finished formulations upon request. The Ancotil suppliers may include Ancotil API manufacturers, exporters, distributors and traders.
click here to find a list of Ancotil 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 Ancotil Drug Master File in Japan (Ancotil JDMF) empowers Ancotil 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 Ancotil JDMF during the approval evaluation for pharmaceutical products. At the time of Ancotil 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 Ancotil suppliers with JDMF on PharmaCompass.
