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) 084292
Active Ingredient(s):
BUTABARBITAL SODIUM
Company:
SANDOZ
Label History
Labels are not available on this site for BUTABARBITAL SODIUM, (ANDA) 084292
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/16/1985
065
Chemistry
6/5/1984
063
Chemistry
6/5/1984
062
Chemistry
7/21/1983
061
Chemistry
7/21/1983
060
Chemistry
5/16/1983
059
Chemistry
6/3/1983
057
Chemistry
3/30/1983
055
Chemistry
2/9/1982
052
Chemistry
2/9/1982
051
Chemistry
2/9/1982
050
Chemistry
Therapeutic Equivalents
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