"57894-030-01" National Drug Code (NDC)

NDC Code	57894-030-01
Package Description	1 VIAL, SINGLE-USE in 1 BOX (57894-030-01) > 10 mL in 1 VIAL, SINGLE-USE
Product NDC	57894-030
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Remicade
Non-Proprietary Name	Infliximab
Dosage Form	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	19980824
Marketing Category Name	BLA
Application Number	BLA103772
Manufacturer	Janssen Biotech, Inc.
Substance Name	INFLIXIMAB
Strength	100
Strength Unit	mg/10mL
Pharmacy Classes	Tumor Necrosis Factor Blocker [EPC], Tumor Necrosis Factor Receptor Blocking Activity [MoA]