DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DIMETANE-TEN
FDA Application No:
(NDA) 011418
Active Ingredient(s):
BROMPHENIRAMINE MALEATE
Company:
WYETH AYERST
Label History
Labels are not available on this site for DIMETANETEN, (NDA) 011418
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/3/1992
025
Control Supplement
6/16/1988
023
Control Supplement
8/13/1986
022
Control Supplement
6/6/1984
021
Control Supplement
12/18/1981
019
Control Supplement
6/6/1981
018
Control Supplement
11/21/1980
017
Labeling Revision
2/1/1980
016
Control Supplement
6/26/1979
015
Labeling Revision
6/26/1979
014
Control Supplement
12/7/1978
013
Control Supplement
5/15/1978
012
Control Supplement
8/26/1977
011
Labeling Revision
9/29/1958
000
Approval
Therapeutic Equivalents
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