DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PENTAZOCINE AND NALOXONE HYDROCHLORIDES
FDA Application No:
(ANDA) 075523
Active Ingredient(s):
NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE
Company:
RANBAXY
Label History
Labels are not available on this site for PENTAZOCINE AND NALOXONE HYDROCHLORIDES, (ANDA) 075523
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/17/2000
000
Approval
Letter
Review
There are no Therapeutic Equivalents
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