"57894-200-01" National Drug Code (NDC)

NDC Code	57894-200-01
Package Description	1 VIAL, SINGLE-USE in 1 BOX (57894-200-01) > 5 mL in 1 VIAL, SINGLE-USE
Product NDC	57894-200
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Reopro
Non-Proprietary Name	Abciximab
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20170103
Marketing Category Name	BLA
Application Number	BLA103575
Manufacturer	Janssen Biotech, Inc.
Substance Name	ABCIXIMAB
Strength	2
Strength Unit	mg/mL