DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FLUOXETINE
FDA Application No:
(ANDA) 075690
Active Ingredient(s):
FLUOXETINE HYDROCHLORIDE
Company:
ACTAVIS MID ATLANTIC
Original Approval or Tentative Approval Date:
January 31, 2002
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
FLUOXETINE
FLUOXETINE HYDROCHLORIDE
EQ 20MG BASE/5ML
SOLUTION; ORAL
Prescription
No
AA
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