"0591-3551-01" National Drug Code (NDC)

NDC Code	0591-3551-01
Package Description	100 TABLET in 1 BOTTLE, PLASTIC (0591-3551-01)
Product NDC	0591-3551
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Oxycodone And Aspirin
Non-Proprietary Name	Oxycodone And Aspirin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20111018
End Marketing Date	20200630
Marketing Category Name	ANDA
Application Number	ANDA090084
Manufacturer	Actavis Pharma, Inc.
Substance Name	OXYCODONE HYDROCHLORIDE; ASPIRIN
Strength	4.8355; 325
Strength Unit	mg/1; mg/1
Pharmacy Classes	Full Opioid Agonists [MoA],Opioid Agonist [EPC],Platelet Aggregation Inhibitor [EPC],Decreased Platelet Aggregation [PE],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
DEA Schedule	CII