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PharmaCompass offers a list of Azathioprine 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 Azathioprine manufacturer or Azathioprine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azathioprine manufacturer or Azathioprine supplier.
PharmaCompass also assists you with knowing the Azathioprine API Price utilized in the formulation of products. Azathioprine API Price is not always fixed or binding as the Azathioprine Price is obtained through a variety of data sources. The Azathioprine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Azathioprine Sodium USP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azathioprine Sodium USP, including repackagers and relabelers. The FDA regulates Azathioprine Sodium USP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azathioprine Sodium USP 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 Azathioprine Sodium USP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azathioprine Sodium USP supplier is an individual or a company that provides Azathioprine Sodium USP active pharmaceutical ingredient (API) or Azathioprine Sodium USP finished formulations upon request. The Azathioprine Sodium USP suppliers may include Azathioprine Sodium USP API manufacturers, exporters, distributors and traders.
click here to find a list of Azathioprine Sodium USP 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 Azathioprine Sodium USP Drug Master File in Japan (Azathioprine Sodium USP JDMF) empowers Azathioprine Sodium USP 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 Azathioprine Sodium USP JDMF during the approval evaluation for pharmaceutical products. At the time of Azathioprine Sodium USP 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 Azathioprine Sodium USP suppliers with JDMF on PharmaCompass.
We have 1 companies offering Azathioprine Sodium USP
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