"71862-007-01" National Drug Code (NDC)

NDC Code	71862-007-01
Package Description	100 TABLET in 1 BOTTLE (71862-007-01)
Product NDC	71862-007
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20171201
Marketing Category Name	ANDA
Application Number	ANDA202413
Manufacturer	Landmark Supply Inc.
Substance Name	IBUPROFEN
Strength	800
Strength Unit	mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]