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01 1URIDINE, 5-BROMO-2' -DEOXY. THIS INFO WAS SUBMITTED NCI/NIH
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4125
Submission : 1981-02-28
Status : Inactive
Type : II
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A Mls002702842 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mls002702842, including repackagers and relabelers. The FDA regulates Mls002702842 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mls002702842 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 Mls002702842 supplier is an individual or a company that provides Mls002702842 active pharmaceutical ingredient (API) or Mls002702842 finished formulations upon request. The Mls002702842 suppliers may include Mls002702842 API manufacturers, exporters, distributors and traders.
click here to find a list of Mls002702842 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mls002702842 DMF (Drug Master File) is a document detailing the whole manufacturing process of Mls002702842 active pharmaceutical ingredient (API) in detail. Different forms of Mls002702842 DMFs exist exist since differing nations have different regulations, such as Mls002702842 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Mls002702842 DMF submitted to regulatory agencies in the US is known as a USDMF. Mls002702842 USDMF includes data on Mls002702842's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Mls002702842 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Mls002702842 suppliers with USDMF on PharmaCompass.
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