"37835-571-05" National Drug Code (NDC)

NDC Code	37835-571-05
Package Description	500 TABLET, DELAYED RELEASE in 1 BOTTLE (37835-571-05)
Product NDC	37835-571
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Adult Low Dose Enteric Coated Aspirin
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20250301
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	Bi-Mart
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]