Visitor Monitoring Drug Details: KALETRA
 
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Drug Details

Drug Name: KALETRA
FDA Application No: (NDA) 021906
Active Ingredient(s): LOPINAVIR; RITONAVIR
Company: ABBOTT
Original Approval or Tentative Approval Date: October 28, 2005
Chemical Type: 3 New dosage form
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
KALETRA LOPINAVIR; RITONAVIR200MG; 50MGTABLET; ORAL Prescription Yes None


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