DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FLUOXETINE
FDA Application No:
(ANDA) 075690
Active Ingredient(s):
FLUOXETINE HYDROCHLORIDE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for FLUOXETINE, (ANDA) 075690
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/17/2002
001
Package Change
1/31/2002
000
Approval
Letter
Other Important Information from FDA
5/10/2001
000
Tentative Approval
Letter
Other Important Information from FDA
Therapeutic Equivalents
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