Visitor Monitoring Drug Details: KANAMYCIN
 
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Drug Details

Drug Name: KANAMYCIN
FDA Application No: (ANDA) 062324
Active Ingredient(s): KANAMYCIN SULFATE
Company: BAXTER HLTHCARE
Original Approval or Tentative Approval Date: November 5, 1981
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
KANAMYCIN KANAMYCIN SULFATEEQ 75MG BASE/2MLINJECTABLE; INJECTION Discontinued No None
KANAMYCIN KANAMYCIN SULFATEEQ 500MG BASE/2MLINJECTABLE; INJECTION Discontinued No None
KANAMYCIN KANAMYCIN SULFATEEQ 1GM BASE/3MLINJECTABLE; INJECTION Discontinued No None


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