"66689-009-50" National Drug Code (NDC)

NDC Code	66689-009-50
Package Description	5 TRAY in 1 CASE (66689-009-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-009-01)
Product NDC	66689-009
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20120816
End Marketing Date	20191130
Marketing Category Name	ANDA
Application Number	ANDA074978
Manufacturer	VistaPharm, Inc.
Substance Name	IBUPROFEN
Strength	100
Strength Unit	mg/5mL
Pharmacy Classes	Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]