"72789-191-20" National Drug Code (NDC)

NDC Code	72789-191-20
Package Description	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-191-20)
Product NDC	72789-191
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180920
Marketing Category Name	ANDA
Application Number	ANDA072096
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	IBUPROFEN
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]