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) 074140
Active Ingredient(s):
NAPROXEN
Company:
SANDOZ
Label History
Labels are not available on this site for NAPROXEN, (ANDA) 074140
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/25/2002
020
Control Supplement
4/19/2002
019
Control Supplement
10/22/2001
018
Control Supplement
10/5/2001
017
Control Supplement
10/5/2001
016
Supplier Addition
11/13/2000
015
Control Supplement
5/5/1999
014
Chemistry
11/13/2000
013
Chemistry
11/13/2000
012
Chemistry
11/13/2000
011
Chemistry
8/17/1998
010
Chemistry
7/14/1998
009
Chemistry
8/17/2000
008
Labeling
8/17/2000
007
Chemistry
10/3/1997
005
Chemistry
5/22/1997
004
Chemistry
12/1/1995
003
Chemistry
1/31/1995
002
Chemistry
1/5/1995
001
Chemistry
12/21/1993
000
Approval
6/30/1993
000
Tentative Approval
Therapeutic Equivalents
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