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 Zoalene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zoalene, including repackagers and relabelers. The FDA regulates Zoalene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zoalene 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 Zoalene supplier is an individual or a company that provides Zoalene active pharmaceutical ingredient (API) or Zoalene finished formulations upon request. The Zoalene suppliers may include Zoalene API manufacturers, exporters, distributors and traders.
click here to find a list of Zoalene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zoalene DMF (Drug Master File) is a document detailing the whole manufacturing process of Zoalene active pharmaceutical ingredient (API) in detail. Different forms of Zoalene DMFs exist exist since differing nations have different regulations, such as Zoalene USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zoalene DMF submitted to regulatory agencies in the US is known as a USDMF. Zoalene USDMF includes data on Zoalene's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zoalene USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zoalene suppliers with USDMF on PharmaCompass.
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