"68382-696-06" National Drug Code (NDC)

NDC Code	68382-696-06
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (68382-696-06)
Product NDC	68382-696
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ritonavir
Non-Proprietary Name	Ritonavir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180320
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA022417
Manufacturer	Zydus Pharmaceuticals USA Inc
Substance Name	RITONAVIR
Strength	100
Strength Unit	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]