DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FLUOXETINE HYDROCHLORIDE
FDA Application No:
(ANDA) 076458
Active Ingredient(s):
FLUOXETINE HYDROCHLORIDE
Company:
PAR PHARM
Label History
Labels are not available on this site for FLUOXETINE HYDROCHLORIDE, (ANDA) 076458
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/14/2004
000
Approval
Review
Other Important Information from FDA
Therapeutic Equivalents
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