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) 070735
Active Ingredient(s):
IBUPROFEN
Company:
SANDOZ
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070735
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/28/2000
019
Package Change
5/12/1989
017
Labeling
1/19/1989
015
Labeling
3/1/1989
014
Chemistry
7/13/1988
012
Labeling
6/29/1988
011
Chemistry
5/17/1988
010
Chemistry
4/13/1988
009
Labeling
4/6/1988
007
Chemistry
11/4/1987
005
Chemistry
7/15/1987
004
Chemistry
7/15/1987
003
Chemistry
7/15/1987
002
Chemistry
5/7/1987
001
Chemistry
6/12/1986
000
Approval
Therapeutic Equivalents
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