"72789-200-90" National Drug Code (NDC)

NDC Code	72789-200-90
Package Description	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-90)
Product NDC	72789-200
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20200821
Marketing Category Name	ANDA
Application Number	ANDA078329
Manufacturer	PD-Rx Pharmaceuticals, 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]