Visitor Monitoring Drug History: KANTREX
 
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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 DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/17/2001 021Facility Addition  
9/2/1998 020Chemistry  
11/29/1990 019Chemistry  
3/6/1975 000Approval  
 
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