DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SODIUM BUTABARBITAL
FDA Application No:
(ANDA) 085418
Active Ingredient(s):
BUTABARBITAL SODIUM
Company:
WEST WARD
Label History
Labels are not available on this site for SODIUM BUTABARBITAL, (ANDA) 085418
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/28/1991
009
Chemistry
8/4/1989
008
Labeling
3/16/1988
007
Labeling
11/8/1982
004
Chemistry
8/15/1977
000
Approval
Therapeutic Equivalents
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