"57237-349-12" National Drug Code (NDC)

NDC Code	57237-349-12
Package Description	120 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-349-12)
Product NDC	57237-349
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Adult Low Dose Aspirin
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20250709
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	Rising Pharma Holdings, Inc.
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]