"72578-065-77" National Drug Code (NDC)

NDC Code	72578-065-77
Package Description	10 BLISTER PACK in 1 CARTON (72578-065-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (72578-065-30)
Product NDC	72578-065
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ranolazine
Non-Proprietary Name	Ranolazine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20190910
Marketing Category Name	ANDA
Application Number	ANDA210188
Manufacturer	Viona Pharmaceuticals Inc
Substance Name	RANOLAZINE
Strength	1000
Strength Unit	mg/1
Pharmacy Classes	Anti-anginal [EPC], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]