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
 
There are no Therapeutic Equivalents Label Information
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
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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