DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TARACTAN
FDA Application No:
(NDA) 016149
Active Ingredient(s):
CHLORPROTHIXENE
Company:
ROCHE
Label History
Labels are not available on this site for TARACTAN, (NDA) 016149
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/29/1981
024
Labeling Revision
1/10/1979
022
Control Supplement
1/10/1979
021
Labeling Revision
5/4/1979
020
Control Supplement
9/10/1976
019
Formulation Revision
6/16/1974
013
Labeling Revision
6/19/1967
000
Approval
There are no Therapeutic Equivalents
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