01 1Cyalume Specialty Products
01 1DICHLORALPHENAZONE USP
01 1U.S.A
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23691
Submission : 2010-04-06
Status : Active
Type : II
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A dichloralphenazone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of dichloralphenazone, including repackagers and relabelers. The FDA regulates dichloralphenazone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. dichloralphenazone 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 dichloralphenazone supplier is an individual or a company that provides dichloralphenazone active pharmaceutical ingredient (API) or dichloralphenazone finished formulations upon request. The dichloralphenazone suppliers may include dichloralphenazone API manufacturers, exporters, distributors and traders.
click here to find a list of dichloralphenazone suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A dichloralphenazone DMF (Drug Master File) is a document detailing the whole manufacturing process of dichloralphenazone active pharmaceutical ingredient (API) in detail. Different forms of dichloralphenazone DMFs exist exist since differing nations have different regulations, such as dichloralphenazone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A dichloralphenazone DMF submitted to regulatory agencies in the US is known as a USDMF. dichloralphenazone USDMF includes data on dichloralphenazone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The dichloralphenazone USDMF is kept confidential to protect the manufacturer’s intellectual property.
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