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) 075452
Active Ingredient(s):
FLUOXETINE HYDROCHLORIDE
Company:
TEVA
Label History
Labels are not available on this site for FLUOXETINE, (ANDA) 075452
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/5/2002
001
Manufacturing Revision
1/29/2002
000
Approval
Letter
Other Important Information from FDA
1/3/2000
000
Tentative Approval
Letter
Other Important Information from FDA
Therapeutic Equivalents
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