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) 074195
Active Ingredient(s):
NAPROXEN SODIUM
Company:
WATSON LABS
Label History
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 074195
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/8/2001
008
Control Supplement
6/8/2001
007
Manufacturing Revision
4/25/2001
006
Control Supplement
12/4/2000
005
Control Supplement
12/4/2000
003
Chemistry
12/4/2000
002
Chemistry
7/13/1995
001
Labeling
12/21/1993
000
Approval
10/28/1992
000
Tentative Approval
Therapeutic Equivalents
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