DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MILTOWN
FDA Application No:
(ANDA) 083919
Active Ingredient(s):
MEPROBAMATE
Company:
MEDPOINTE PHARM HLC
Label History
Labels are not available on this site for MILTOWN, (ANDA) 083919
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/30/1993
015
Chemistry in Effect
4/5/1990
014
Labeling
3/3/1989
013
Chemistry
5/9/1983
010
Chemistry
7/14/1982
008
Chemistry
1/28/1974
000
Approval
Therapeutic Equivalents
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