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) 080655
Active Ingredient(s):
MEPROBAMATE
Company:
SANDOZ
Label History
Labels are not available on this site for MEPROBAMATE, (ANDA) 080655
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/5/1997
089
Chemistry
2/21/1995
088
Chemistry
12/22/1989
087
Labeling
10/18/1989
086
Labeling in Effect
8/4/1989
085
Labeling
3/28/1988
084
Labeling
11/30/1983
081
Chemistry
8/4/1983
080
Chemistry
8/4/1983
079
Chemistry
10/18/1982
078
Chemistry
10/18/1982
077
Chemistry
10/18/1982
076
Chemistry
5/18/1982
075
Chemistry
5/18/1982
073
Chemistry
5/24/1982
071
Chemistry
5/18/1982
069
Chemistry
5/18/1982
062
Chemistry
5/18/1982
061
Chemistry
5/18/1982
042
Chemistry
7/12/1972
000
Approval
Therapeutic Equivalents
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