DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
TALWIN 50
FDA Application No:
(NDA) 016732
Active Ingredient(s):
PENTAZOCINE HYDROCHLORIDE
Company:
SANOFI AVENTIS US
Original Approval or Tentative Approval Date:
February 3, 1969
Chemical Type:
2 New active ingredient
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
TALWIN 50
PENTAZOCINE HYDROCHLORIDE
EQ 50MG BASE
TABLET; ORAL
Discontinued
No
None
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