Kaletra - 49349-024-02 - (Kaletra)

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Drug Information of Kaletra

Product NDC: 49349-024
Proprietary Name: Kaletra
Non Proprietary Name: Kaletra
Active Ingredient(s): 200; 50    mg/1; mg/1 & nbsp;   Kaletra
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Kaletra

Product NDC: 49349-024
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075659
Marketing Category: ANDA
Start Marketing Date: 20100927

Package Information of Kaletra

Package NDC: 49349-024-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-024-02)

NDC Information of Kaletra

NDC Code 49349-024-02
Proprietary Name Kaletra
Package Description 30 TABLET in 1 BLISTER PACK (49349-024-02)
Product NDC 49349-024
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Kaletra
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100927
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LOPINAVIR; RITONAVIR
Strength Number 200; 50
Strength Unit mg/1; mg/1
Pharmaceutical Classes HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC],HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC]

Complete Information of Kaletra


General Information