DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CEFUROXIME
FDA Application No:
(ANDA) 065001
Active Ingredient(s):
CEFUROXIME SODIUM
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for CEFUROXIME, (ANDA) 065001
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/12/2002
002
Labeling
3/28/2002
001
Control Supplement
5/30/2001
000
Approval
Letter
Therapeutic Equivalents
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