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) 083337
Active Ingredient(s):
BUTABARBITAL SODIUM
Company:
WHITEWORTH TOWN PLSN
Label History
Labels are not available on this site for BUTABARBITAL SODIUM, (ANDA) 083337
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/28/1974
000
Approval
Therapeutic Equivalents
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