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) 074162
Active Ingredient(s):
NAPROXEN SODIUM
Company:
SANDOZ
Label History
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 074162
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/19/2002
016
Control Supplement
5/9/2001
015
Control Supplement
8/8/2001
014
Control Supplement
8/29/2001
013
Control Supplement
1/4/2001
012
Control Supplement
4/26/2001
011
Control Supplement
5/5/1999
010
Chemistry
6/29/1998
009
Chemistry
3/9/1998
008
Labeling
3/4/1999
007
Labeling
3/4/1999
006
Chemistry
11/10/1997
005
Labeling
2/4/1998
004
Chemistry
10/17/1997
003
Chemistry
10/17/1997
002
Chemistry
2/27/1996
001
Chemistry
12/21/1993
000
Approval
6/29/1993
000
Tentative Approval
Therapeutic Equivalents
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