"57894-071-89" National Drug Code (NDC)

NDC Code	57894-071-89
Package Description	1 SYRINGE in 1 CARTON (57894-071-89) / 1 mL in 1 SYRINGE
Product NDC	57894-071
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Simponi
Non-Proprietary Name	Golimumab
Dosage Form	INJECTION, SOLUTION
Usage	SUBCUTANEOUS
Start Marketing Date	20130515
Marketing Category Name	BLA
Application Number	BLA125289
Manufacturer	Janssen Biotech, Inc.
Substance Name	GOLIMUMAB
Strength	100
Strength Unit	mg/mL
Pharmacy Classes	Tumor Necrosis Factor Blocker [EPC], Tumor Necrosis Factor Receptor Blocking Activity [MoA]