DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NAPROXEN
FDA Application No:
(ANDA) 075337
Active Ingredient(s):
NAPROXEN
Company:
PLIVA
Label History
Labels are not available on this site for NAPROXEN, (ANDA) 075337
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/1/2002
004
Manufacturing Revision
7/1/2002
003
Control Supplement
7/1/2002
002
Facility Addition
7/7/2000
001
Facility Addition
5/26/1999
000
Approval
Letter
Therapeutic Equivalents
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