"57894-650-02" National Drug Code (NDC)

NDC Code	57894-650-02
Package Description	1 VIAL, SINGLE-DOSE in 1 CARTON (57894-650-02) / 20 mL in 1 VIAL, SINGLE-DOSE (57894-650-01)
Product NDC	57894-650
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tremfya
Non-Proprietary Name	Guselkumab
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20240911
Marketing Category Name	BLA
Application Number	BLA761061
Manufacturer	Janssen Biotech, Inc.
Substance Name	GUSELKUMAB
Strength	200
Strength Unit	mg/20mL
Pharmacy Classes	Interleukin-23 Antagonist [EPC], Interleukin-23 Antagonists [MoA]