"0074-6799-22" National Drug Code (NDC)

Kaletra 120 TABLET, FILM COATED in 1 BOTTLE (0074-6799-22)
(AbbVie Inc.)

NDC Code0074-6799-22
Package Description120 TABLET, FILM COATED in 1 BOTTLE (0074-6799-22)
Product NDC0074-6799
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameKaletra
Non-Proprietary NameLopinavir And Ritonavir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100618
Marketing Category NameNDA
Application NumberNDA021906
ManufacturerAbbVie Inc.
Substance NameLOPINAVIR; RITONAVIR
Strength200; 50
Strength Unitmg/1; mg/1
Pharmacy ClassesBreast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Cytochrome P450 3A Inhibitor [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], HIV Protease Inhibitors [MoA], HIV Protease Inhibitors [MoA], Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA], Protease Inhibitor [EPC], Protease Inhibitor [EPC], UDP Glucuronosyltransferases Inducers [MoA]

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