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) 074495
Active Ingredient(s):
NAPROXEN SODIUM
Company:
SANDOZ
Label History
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 074495
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/4/2000
009
Control Supplement
12/4/2000
008
Supplier Addition
3/27/2000
007
Control Supplement
3/27/2000
006
Control Supplement
3/27/2000
005
Facility Addition
4/29/1996
004
Chemistry
6/24/1996
003
Chemistry
1/19/1996
002
Labeling
12/5/1994
000
Approval
Therapeutic Equivalents
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