"11822-2270-4" National Drug Code (NDC)

NDC Code	11822-2270-4
Package Description	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11822-2270-4)
Product NDC	11822-2270
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Aspirin
Proprietary Name Suffix	Pain Relief
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	19921214
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	Rite Aid Corporation
Substance Name	ASPIRIN
Strength	325
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]