Visitor Monitoring Drug Details: KALETRA
 
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Drug Details

Drug Name: KALETRA
FDA Application No: (NDA) 021226
Active Ingredient(s): LOPINAVIR; RITONAVIR
Company: ABBOTT
Original Approval or Tentative Approval Date: September 15, 2000
Chemical Type: 14 New molecular entity and new combination
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; RITONAVIR133.3MG; 33.3MGCAPSULE; ORAL Prescription Yes None


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