"71679-301-05" National Drug Code (NDC)

NDC Code	71679-301-05
Package Description	500 TABLET, DELAYED RELEASE in 1 BOTTLE (71679-301-05)
Product NDC	71679-301
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Aspirin
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20240307
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	Health Pharma USA, LLC
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]