"70518-1519-0" National Drug Code (NDC)

NDC Code	70518-1519-0
Package Description	30 TABLET in 1 BLISTER PACK (70518-1519-0)
Product NDC	70518-1519
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ritonavir
Non-Proprietary Name	Ritonavir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20181011
Marketing Category Name	ANDA
Application Number	ANDA204587
Manufacturer	REMEDYREPACK 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]