"21695-362-12" National Drug Code (NDC)

NDC Code	21695-362-12
Package Description	12 TABLET, FILM COATED in 1 BOTTLE (21695-362-12)
Product NDC	21695-362
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Kaletra
Non-Proprietary Name	Lopinavir And Ritonavir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20100618
Marketing Category Name	NDA
Application Number	NDA021906
Manufacturer	Rebel Distributors Corp
Substance Name	LOPINAVIR; RITONAVIR
Strength	200; 50
Strength Unit	mg/1; mg/1
Pharmacy Classes	HIV Protease Inhibitors [MoA],Cytochrome P450 3A Inhibitor [EPC],Protease Inhibitor [EPC],Cytochrome P450 3A Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],P-Glycoprotein Inhibitors [MoA],Breast Cancer Resistance Protein Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],UDP Glucuronosyltransferases Inducers [MoA],HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC],P-Glycoprotein Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA],Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA]