DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
IBUPROFEN
FDA Application No:
(ANDA) 072199
Active Ingredient(s):
IBUPROFEN
Company:
INTERPHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 072199
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/22/2002
022
Labeling
9/25/2001
021
Manufacturing Revision
5/21/2001
020
Labeling
3/13/2001
019
Labeling
12/6/2000
018
Facility Addition
4/12/2000
017
Control Supplement
4/12/2000
016
Manufacturing Revision
9/15/1999
015
Labeling
4/12/2000
014
Facility Addition
9/24/1999
012
Chemistry
2/11/1999
011
Chemistry
8/1/2000
010
Labeling
8/1/2000
009
Chemistry
8/1/2000
008
Chemistry
8/1/2000
007
Chemistry
7/24/1997
005
Chemistry
11/22/1994
004
Labeling
1/20/1998
003
Chemistry
5/23/1988
000
Approval
Therapeutic Equivalents
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