Visitor Monitoring Drug Details: ELOXATIN
 
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Drug Details

Drug Name: ELOXATIN
FDA Application No: (NDA) 021759
Active Ingredient(s): OXALIPLATIN
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: January 31, 2005
Chemical Type: 5 New manufacturer
Review Classification: P Priority review drug
 
 
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
ELOXATIN OXALIPLATIN50MG/10ML (5MG/ML)INJECTABLE; IV (INFUSION) Prescription Yes None
ELOXATIN OXALIPLATIN100MG/20ML (5MG/ML)INJECTABLE; IV (INFUSION) Prescription Yes None
ELOXATIN OXALIPLATIN200MG/40ML (5MG/ML)INJECTABLE; IV (INFUSION) Prescription Yes None


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