"41163-522-02" National Drug Code (NDC)

NDC Code	41163-522-02
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (41163-522-02) / 125 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product NDC	41163-522
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Aspirin
Proprietary Name Suffix	Regular Strength
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20141001
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	United Natural Foods, Inc. dba UNFI
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]