DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PROZAC
FDA Application No:
(NDA) 020101
Active Ingredient(s):
FLUOXETINE HYDROCHLORIDE
Company:
LILLY
Original Approval or Tentative Approval Date:
April 24, 1991
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
PROZAC
FLUOXETINE HYDROCHLORIDE
EQ 20MG BASE/5ML
SOLUTION; ORAL
Prescription
Yes
AA
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