"68071-5102-0" National Drug Code (NDC)

NDC Code	68071-5102-0
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (68071-5102-0)
Product NDC	68071-5102
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Yosprala
Non-Proprietary Name	Yosprala
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20190717
Marketing Category Name	NDA
Application Number	NDA205103
Manufacturer	NuCare Pharmaceuticals,Inc.
Substance Name	ASPIRIN; OMEPRAZOLE
Strength	81; 40
Strength Unit	mg/1; mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]