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) 076642
Active Ingredient(s):
HYDROCODONE BITARTRATE; IBUPROFEN
Company:
INTERPHARM
Label History
Labels are not available on this site for HYDROCODONE BITARTRATE AND IBUPROFEN, (ANDA) 076642
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/19/2007
008
Labeling
Letter
10/19/2007
007
Chemistry New Strength
Letter
10/19/2007
006
Labeling
Letter
10/19/2007
005
Chemistry New Strength
Letter
10/12/2004
003
Supplement
3/18/2004
000
Tentative Approval
3/18/2004
000
Approval
There are no Therapeutic Equivalents
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