"72606-059-01" National Drug Code (NDC)

NDC Code	72606-059-01
Package Description	1 VIAL, SINGLE-USE in 1 CARTON (72606-059-01) / 1.7 mL in 1 VIAL, SINGLE-USE
Product NDC	72606-059
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Denosumab-bmwo
Non-Proprietary Name	Denosumab-bmwo
Dosage Form	INJECTION
Usage	SUBCUTANEOUS
Start Marketing Date	20250910
Marketing Category Name	BLA
Application Number	BLA761404
Manufacturer	CELLTRION USA, Inc.
Substance Name	DENOSUMAB
Strength	120
Strength Unit	mg/1.7mL
Pharmacy Classes	RANK Ligand Blocking Activity [MoA], RANK Ligand Inhibitor [EPC]