"50804-880-04" National Drug Code (NDC)

NDC Code	50804-880-04
Package Description	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (50804-880-04)
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 NOT FINAL
Application Number	part343
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]