"67457-978-50" National Drug Code (NDC)

NDC Code	67457-978-50
Package Description	1 VIAL, GLASS in 1 CARTON (67457-978-50) / 25 mL in 1 VIAL, GLASS
Product NDC	67457-978
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Aloprim
Non-Proprietary Name	Allopurinol
Dosage Form	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20201118
End Marketing Date	20251130
Marketing Category Name	NDA
Application Number	NDA020298
Manufacturer	Mylan Institutional LLC
Substance Name	ALLOPURINOL SODIUM
Strength	500
Strength Unit	mg/25mL
Pharmacy Classes	Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]