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) 070330
Active Ingredient(s):
IBUPROFEN
Company:
PAR PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070330
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/13/1998
037
Chemistry
1/14/1997
035
Chemistry
4/29/1994
032
Chemistry
3/7/1994
031
Chemistry in Effect
1/10/1992
030
Labeling
6/11/1991
029
Labeling
2/21/1989
027
Labeling
3/2/1989
025
Chemistry
10/26/1988
024
SBA
11/22/1988
024
Chemistry
3/2/1989
023
Chemistry
3/2/1989
022
Chemistry
12/31/1987
018
Chemistry
2/10/1988
017
Chemistry
9/22/1987
016
Chemistry
9/22/1987
015
Chemistry
2/2/1988
014
Chemistry
2/2/1988
013
Chemistry
7/22/1987
010
Chemistry
6/11/1986
008
Chemistry
5/16/1986
007
Chemistry
12/26/1985
003
Chemistry
8/6/1985
000
Approval
Therapeutic Equivalents
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