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) 076006
Active Ingredient(s):
FLUOXETINE HYDROCHLORIDE
Company:
DR REDDYS LABS INC
Label History
Labels are not available on this site for FLUOXETINE HYDROCHLORIDE, (ANDA) 076006
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/30/2002
000
Approval
Other Important Information from FDA
8/23/2001
000
Tentative Approval
Other Important Information from FDA
Therapeutic Equivalents
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