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) 083308
Active Ingredient(s):
MEPROBAMATE
Company:
WATSON LABS
Label History
Labels are not available on this site for MEPROBAMATE, (ANDA) 083308
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2001
049
Control Supplement
1/20/1998
047
Chemistry
1/20/1998
046
Chemistry
1/28/1991
044
Chemistry
8/7/1991
043
Chemistry
6/29/1990
042
Chemistry
2/8/1989
041
Labeling
10/26/1988
040
SBA
10/13/1988
040
Labeling
10/21/1988
039
Chemistry
10/21/1988
038
Chemistry
6/2/1982
036
Chemistry
6/2/1982
035
Chemistry
5/3/1973
000
Approval
Therapeutic Equivalents
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