DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DEMAZIN
FDA Application No:
(NDA) 018556
Active Ingredient(s):
CHLORPHENIRAMINE MALEATE; PHENYLPROPANOLAMINE HYDROCHLORIDE
Company:
SCHERING PLOUGH
Label History
Labels are not available on this site for DEMAZIN, (NDA) 018556
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/8/1986
003
Control Supplement
11/20/1985
002
Control Supplement
9/18/1984
001
Package Change
5/14/1984
000
Approval
There are no Therapeutic Equivalents
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