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:
(NDA) 015417
Active Ingredient(s):
MEPROBAMATE
Company:
WEST WARD
Label History
Labels are not available on this site for MEPROBAMATE, (NDA) 015417
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/11/1981
012
Labeling Revision
8/26/1977
010
Labeling Revision
12/12/1964
000
Approval
Therapeutic Equivalents
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