DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NAPROXEN SODIUM
FDA Application No:
(ANDA) 074230
Active Ingredient(s):
NAPROXEN SODIUM
Company:
IVAX PHARMS
Label History
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 074230
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/29/2002
003
Facility Addition
1/28/2000
002
Facility Addition
12/2/1996
001
Labeling
3/14/1995
000
Approval
Therapeutic Equivalents
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