"43063-890-50" National Drug Code (NDC)

NDC Code	43063-890-50
Package Description	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-890-50)
Product NDC	43063-890
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