DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PAXIL
FDA Application No:
(NDA) 020885
Active Ingredient(s):
PAROXETINE HYDROCHLORIDE
Company:
GLAXOSMITHKLINE
Label History
Labels are not available on this site for PAXIL, (NDA) 020885
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/30/2001
004
Manufacturing Change or Addition
4/30/2001
003
Manufacturing Change or Addition
7/18/2000
002
Manufacturing Change or Addition
9/21/2000
001
Control Supplement
10/9/1998
000
Approval
Letter
Review
Other Important Information from FDA
There are no Therapeutic Equivalents
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