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) 080699
Active Ingredient(s):
MEPROBAMATE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for MEPROBAMATE, (ANDA) 080699
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
130
Chemistry
12/23/1994
129
Chemistry
4/3/1992
128
Chemistry
4/3/1992
126
Chemistry
4/3/1992
125
Chemistry
4/3/1992
124
Chemistry
4/3/1992
123
Chemistry
3/15/1989
122
Labeling
10/13/1988
121
Labeling
3/12/1986
118
Chemistry
10/16/1972
000
Approval
Therapeutic Equivalents
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