DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HYDROCODONE BITARTRATE AND IBUPROFEN
FDA Application No:
(ANDA) 077727
Active Ingredient(s):
HYDROCODONE BITARTRATE; IBUPROFEN
Company:
VINTAGE PHARMS
Label History
Labels are not available on this site for HYDROCODONE BITARTRATE AND IBUPROFEN, (ANDA) 077727
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/6/2006
000
Approval
There are no Therapeutic Equivalents
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