"68308-845-01" National Drug Code (NDC)

NDC Code	68308-845-01
Package Description	100 TABLET in 1 BOTTLE, PLASTIC (68308-845-01)
Product NDC	68308-845
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Oxycodone And Aspirin
Non-Proprietary Name	Oxycodone Hydrochloride And Aspirin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20110502
End Marketing Date	20210630
Marketing Category Name	ANDA
Application Number	ANDA091670
Manufacturer	Mayne 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