"69448-019-26" National Drug Code (NDC)

NDC Code	69448-019-26
Package Description	1 VIAL, SINGLE-USE in 1 CARTON (69448-019-26) / 26 mL in 1 VIAL, SINGLE-USE
Product NDC	69448-019
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Imuldosa
Non-Proprietary Name	Ustekinumab-srlf
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20241018
Marketing Category Name	BLA
Application Number	BLA761364
Manufacturer	Accord BioPharma Inc.
Substance Name	USTEKINUMAB
Strength	130
Strength Unit	mg/26mL
Pharmacy Classes	Interleukin-12 Antagonist [EPC], Interleukin-12 Antagonists [MoA], Interleukin-23 Antagonist [EPC], Interleukin-23 Antagonists [MoA]