"60687-364-25" National Drug Code (NDC)

NDC Code	60687-364-25
Package Description	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-364-25) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-364-95)
Product NDC	60687-364
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ritonavir
Non-Proprietary Name	Ritonavir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180501
End Marketing Date	20191031
Marketing Category Name	ANDA
Application Number	ANDA202573
Manufacturer	American Health Packaging
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]