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) 074289
Active Ingredient(s):
NAPROXEN SODIUM
Company:
TEVA PHARMS
Label History
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 074289
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/23/1999
005
Chemistry
10/18/1996
004
Labeling
5/31/1996
003
Chemistry
3/22/1996
002
Labeling
6/28/1994
001
Chemistry
1/27/1994
000
Approval
Therapeutic Equivalents
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