DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DIDREX
FDA Application No:
(NDA) 012427
Active Ingredient(s):
BENZPHETAMINE HYDROCHLORIDE
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for DIDREX, (NDA) 012427
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/23/1998
023
Package Change
7/31/1992
022
Control Supplement
7/28/2000
021
Labeling Revision
7/27/2000
020
Labeling Revision
12/31/1985
019
Labeling Revision
9/4/1984
018
Labeling Revision
10/26/1960
000
Approval
Therapeutic Equivalents
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