DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
TALWIN NX
FDA Application No:
(NDA) 018733
Active Ingredient(s):
NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE
Company:
SANOFI AVENTIS US
Original Approval or Tentative Approval Date:
December 16, 1982
Chemical Type:
4 New combination
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
Labels are not available
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
TALWIN NX
NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE
EQ 0.5MG BASE; EQ 50MG BASE
TABLET; ORAL
Prescription
Yes
AB
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