DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
UREX
FDA Application No:
(NDA) 016151
Active Ingredient(s):
METHENAMINE HIPPURATE
Company:
VATRING PHARMS
Label History
Labels are not available on this site for UREX, (NDA) 016151
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/2/1993
023
Manufacturing Change or Addition
8/10/1988
021
Manufacturing Change or Addition
11/10/1992
020
Labeling Revision
4/21/1986
019
Labeling Revision
3/6/1989
018
Practioner Draft Labeling
7/24/1975
015
Control Supplement
7/5/1967
000
Approval
Therapeutic Equivalents
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