DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
KETOCONAZOLE
FDA Application No:
(ANDA) 075597
Active Ingredient(s):
KETOCONAZOLE
Company:
MYLAN
Label History
Labels are not available on this site for KETOCONAZOLE, (ANDA) 075597
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/16/2007
001
Control Supplement
12/23/1999
000
Approval
Letter
Therapeutic Equivalents
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