"83654-105-01" National Drug Code (NDC)

NDC Code	83654-105-01
Package Description	1 VIAL, SINGLE-DOSE in 1 BOX (83654-105-01) / 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC	83654-105
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Penpulimab
Proprietary Name Suffix	Kcqx
Non-Proprietary Name	Penpulimab
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20250423
Marketing Category Name	BLA
Application Number	BLA761258
Manufacturer	Akeso Biopharma, Co., Ltd
Substance Name	PENPULIMAB
Strength	100
Strength Unit	mg/10mL