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) 076117
Active Ingredient(s):
IBUPROFEN
Company:
DR REDDYS LABS INC
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 076117
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/1/2002
001
Package Change
11/20/2001
000
Approval
Letter
Review
Therapeutic Equivalents
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