01 GSK (1)
02 Roche Diagnostics GmbH (1)
03 SIGMA TAU (1)
04 Blank (1)
01 5-BROMO-2'-DEOXYURIDINE (2)
02 5-FLUORO-2'-DEOXYURIDINE (1)
03 5-IODO-2-DEOXYURIDINE (IUDR) (1)
01 Germany (1)
02 U.S.A (1)
03 United Kingdom (1)
04 Blank (1)
01 Inactive (4)
01 Blank (4)
19
PharmaCompass offers a list of Deoxyuridine 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 Deoxyuridine manufacturer or Deoxyuridine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deoxyuridine manufacturer or Deoxyuridine supplier.
PharmaCompass also assists you with knowing the Deoxyuridine API Price utilized in the formulation of products. Deoxyuridine API Price is not always fixed or binding as the Deoxyuridine Price is obtained through a variety of data sources. The Deoxyuridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deoxyuridine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deoxyuridine, including repackagers and relabelers. The FDA regulates Deoxyuridine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deoxyuridine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Deoxyuridine supplier is an individual or a company that provides Deoxyuridine active pharmaceutical ingredient (API) or Deoxyuridine finished formulations upon request. The Deoxyuridine suppliers may include Deoxyuridine API manufacturers, exporters, distributors and traders.
click here to find a list of Deoxyuridine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Deoxyuridine DMF (Drug Master File) is a document detailing the whole manufacturing process of Deoxyuridine active pharmaceutical ingredient (API) in detail. Different forms of Deoxyuridine DMFs exist exist since differing nations have different regulations, such as Deoxyuridine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Deoxyuridine DMF submitted to regulatory agencies in the US is known as a USDMF. Deoxyuridine USDMF includes data on Deoxyuridine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Deoxyuridine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Deoxyuridine suppliers with USDMF on PharmaCompass.
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