DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FLOXURIDINE
FDA Application No:
(ANDA) 075837
Active Ingredient(s):
FLOXURIDINE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for FLOXURIDINE, (ANDA) 075837
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/5/2002
004
Facility Addition
11/26/2002
003
Control Supplement
11/26/2002
002
Manufacturing Revision
11/26/2002
001
Facility Addition
2/22/2001
000
Approval
Letter
Review
Therapeutic Equivalents
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