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) 072169
Active Ingredient(s):
IBUPROFEN
Company:
SANDOZ
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 072169
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/28/2000
008
Package Change
1/19/1989
006
Labeling
4/26/1989
005
Chemistry
7/25/1988
003
Labeling
6/30/1988
002
Chemistry
4/7/1988
001
Labeling
12/11/1987
000
Approval
Therapeutic Equivalents
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