DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
IBUPROHM
FDA Application No:
(ANDA) 071214
Active Ingredient(s):
IBUPROFEN
Company:
OHM LABS
Label History
Labels are not available on this site for IBUPROHM, (ANDA) 071214
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/17/1999
013
Labeling
9/17/1999
012
Labeling
8/5/1994
011
Chemistry
9/21/1992
010
Chemistry
9/21/1992
009
Chemistry
3/13/1992
008
Chemistry
1/10/1989
006
Chemistry
6/3/1988
005
Chemistry
10/28/1987
004
Chemistry
10/28/1987
003
Chemistry
12/9/1987
001
Chemistry
12/1/1986
000
Approval
Therapeutic Equivalents
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