Kaletra - 0074-3956-46 - (Lopinavir and Ritonavir)

Alphabetical Index


Drug Information of Kaletra

Product NDC: 0074-3956
Proprietary Name: Kaletra
Non Proprietary Name: Lopinavir and Ritonavir
Active Ingredient(s): 80; 20    mg/mL; mg/mL & nbsp;   Lopinavir and Ritonavir
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kaletra

Product NDC: 0074-3956
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021251
Marketing Category: NDA
Start Marketing Date: 20100618

Package Information of Kaletra

Package NDC: 0074-3956-46
Package Description: 160 mL in 1 BOTTLE (0074-3956-46)

NDC Information of Kaletra

NDC Code 0074-3956-46
Proprietary Name Kaletra
Package Description 160 mL in 1 BOTTLE (0074-3956-46)
Product NDC 0074-3956
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lopinavir and Ritonavir
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20100618
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name LOPINAVIR; RITONAVIR
Strength Number 80; 20
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC],HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC]

Complete Information of Kaletra


General Information