DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
KANTREX
FDA Application No:
(ANDA) 061901
Active Ingredient(s):
KANAMYCIN SULFATE
Company:
APOTHECON
Label History
Labels are not available on this site for KANTREX, (ANDA) 061901
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/17/2001
021
Facility Addition
9/2/1998
020
Chemistry
11/29/1990
019
Chemistry
3/6/1975
000
Approval
Therapeutic Equivalents
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