DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ACETAMINOPHEN AND PENTAZOCINE HYDROCHLORIDE
FDA Application No:
(ANDA) 076202
Active Ingredient(s):
ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE
Company:
ACTAVIS TOTOWA
Label History
Labels are not available on this site for ACETAMINOPHEN AND PENTAZOCINE HYDROCHLORIDE, (ANDA) 076202
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/2/2002
000
Approval
There are no Therapeutic Equivalents
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