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) 070734
Active Ingredient(s):
IBUPROFEN
Company:
SANDOZ
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070734
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/28/2000
002
Package Change
1/24/1994
001
Chemistry
6/12/1986
000
Approval
Therapeutic Equivalents
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