"50804-880-01" National Drug Code (NDC)

NDC Code	50804-880-01
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (50804-880-01) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product NDC	50804-880
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Aspirin
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20190101
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	GOODSENSE
Substance Name	ASPIRIN
Strength	81
Strength Unit	mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]