01 1GSK
02 1Roche Diagnostics GmbH
03 1SIGMA TAU
04 1Blank
01 25-BROMO-2'-DEOXYURIDINE
02 15-FLUORO-2'-DEOXYURIDINE
03 15-IODO-2-DEOXYURIDINE (IUDR)
01 1Germany
02 1U.S.A
03 1United Kingdom
04 1Blank
01 4Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 532
Submission : 1963-04-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12277
Submission : 1996-12-16
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4324
Submission : 1981-10-01
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6502
Submission : 1986-07-18
Status : Inactive
Type : II
Portfolio PDF
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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 DUR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DUR, including repackagers and relabelers. The FDA regulates DUR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DUR 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 DUR supplier is an individual or a company that provides DUR active pharmaceutical ingredient (API) or DUR finished formulations upon request. The DUR suppliers may include DUR API manufacturers, exporters, distributors and traders.
click here to find a list of DUR suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DUR DMF (Drug Master File) is a document detailing the whole manufacturing process of DUR active pharmaceutical ingredient (API) in detail. Different forms of DUR DMFs exist exist since differing nations have different regulations, such as DUR USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DUR DMF submitted to regulatory agencies in the US is known as a USDMF. DUR USDMF includes data on DUR's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DUR USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DUR suppliers with USDMF on PharmaCompass.
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