DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BUTABARBITAL SODIUM
FDA Application No:
(ANDA) 085934
Active Ingredient(s):
BUTABARBITAL SODIUM
Company:
SANDOZ
Label History
Labels are not available on this site for BUTABARBITAL SODIUM, (ANDA) 085934
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/11/1983
011
Chemistry
11/12/1982
010
Chemistry
5/28/1985
009
Chemistry
7/17/1978
000
Approval
Therapeutic Equivalents
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