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) 074201
Active Ingredient(s):
NAPROXEN
Company:
TEVA
Label History
Labels are not available on this site for NAPROXEN, (ANDA) 074201
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/22/2001
018
Package Change
10/22/2001
017
Package Change
12/13/2000
016
Manufacturing Revision
8/28/2000
014
Facility Addition
12/2/1999
013
Facility Addition
12/2/1999
012
Facility Addition
2/12/1999
007
Chemistry
2/12/1999
006
Chemistry
8/16/1996
005
Chemistry
10/29/1996
004
Chemistry
3/13/1996
003
Labeling
1/27/1995
002
Chemistry
10/21/1994
001
Chemistry
12/21/1993
000
Approval
5/27/1993
000
Tentative Approval
Therapeutic Equivalents
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