"71205-517-60" National Drug Code (NDC)

NDC Code	71205-517-60
Package Description	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-60)
Product NDC	71205-517
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Tri-buffered Aspirin
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	19900330
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	Proficient Rx LP
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]