DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEPROBAMATE
FDA Application No:
(ANDA) 083304
Active Ingredient(s):
MEPROBAMATE
Company:
WATSON LABS
Label History
Labels are not available on this site for MEPROBAMATE, (ANDA) 083304
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2001
041
Control Supplement
1/28/1991
039
Chemistry
6/29/1990
037
Chemistry
2/8/1989
036
Labeling
10/26/1988
035
SBA
10/25/1988
035
Labeling
9/23/1988
034
Chemistry
9/23/1988
033
Chemistry
12/12/1985
031
Chemistry
5/14/1985
030
Chemistry
5/14/1985
029
Chemistry
4/23/1973
000
Approval
There are no Therapeutic Equivalents
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