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) 073343
Active Ingredient(s):
IBUPROFEN
Company:
TEVA
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 073343
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/2/1999
010
Facility Addition
12/2/1999
009
Facility Addition
2/12/1999
004
Chemistry
2/12/1999
003
Chemistry
8/28/1998
002
Chemistry
2/3/1993
001
Chemistry
6/30/1992
000
Approval
Therapeutic Equivalents
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