01 1The Dow Chemical Company
01 1ZOALENE W/ARSANILIC ACID OR SODIUM ARSANILATE IN MEDICATED FEED (VET)
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 700
Submission : 1963-10-25
Status : Inactive
Type : II
A Dinitolmide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dinitolmide, including repackagers and relabelers. The FDA regulates Dinitolmide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dinitolmide 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 Dinitolmide supplier is an individual or a company that provides Dinitolmide active pharmaceutical ingredient (API) or Dinitolmide finished formulations upon request. The Dinitolmide suppliers may include Dinitolmide API manufacturers, exporters, distributors and traders.
click here to find a list of Dinitolmide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dinitolmide DMF (Drug Master File) is a document detailing the whole manufacturing process of Dinitolmide active pharmaceutical ingredient (API) in detail. Different forms of Dinitolmide DMFs exist exist since differing nations have different regulations, such as Dinitolmide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dinitolmide DMF submitted to regulatory agencies in the US is known as a USDMF. Dinitolmide USDMF includes data on Dinitolmide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dinitolmide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dinitolmide suppliers with USDMF on PharmaCompass.
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