"61755-001-01" National Drug Code (NDC)

NDC Code	61755-001-01
Package Description	4 VIAL, SINGLE-USE in 1 CARTON (61755-001-01) > 2 mL in 1 VIAL, SINGLE-USE
Product NDC	61755-001
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Arcalyst
Non-Proprietary Name	Rilonacept
Dosage Form	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage	SUBCUTANEOUS
Start Marketing Date	20080227
End Marketing Date	20220131
Marketing Category Name	BLA
Application Number	BLA125249
Manufacturer	Regeneron Pharmaceuticals, Inc.
Substance Name	RILONACEPT
Strength	160
Strength Unit	mg/2mL