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) 070435
Active Ingredient(s):
IBUPROFEN
Company:
WATSON LABS
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070435
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/8/1989
035
SBA
11/19/1990
018
Chemistry
6/29/1990
016
Chemistry
3/8/1989
015
SBA
1/30/1992
015
Chemistry
1/30/1992
014
Chemistry
1/30/1992
013
Chemistry
9/23/1992
012
Chemistry
10/20/1986
010
Chemistry
10/20/1986
009
Chemistry
10/20/1986
007
Chemistry
10/20/1986
006
Chemistry
8/25/1986
004
Chemistry
3/25/1986
002
Chemistry
4/30/1986
001
Chemistry
3/5/1986
000
Approval
Therapeutic Equivalents
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