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) 071268
Active Ingredient(s):
IBUPROFEN
Company:
LEINER
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071268
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/23/1989
012
Labeling
12/18/1987
010
Chemistry
12/18/1987
009
Chemistry
12/18/1987
008
Chemistry
7/6/1987
007
Chemistry
7/6/1987
006
Chemistry
7/6/1987
005
Chemistry
10/2/1987
004
Chemistry
1/21/1987
003
Chemistry
5/14/1987
002
Chemistry
5/14/1987
001
Chemistry
10/15/1986
000
Approval
Therapeutic Equivalents
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