"59779-439-51" National Drug Code (NDC)

NDC Code	59779-439-51
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (59779-439-51) / 365 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product NDC	59779-439
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Aspirin
Proprietary Name Suffix	Low Strength, Enteric
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20130503
End Marketing Date	20250523
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	CVS Pharmacy
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]