Package 50242-201-01

Brand: lunsumio velo

Generic: mosunetuzumab
NDC Package

Package Facts

Identity

Package NDC 50242-201-01
Digits Only 5024220101
Product NDC 50242-201
Product ID 50242-201_9f54a0a1-d24b-429e-9a1b-393ed834f1a6
Description

1 VIAL, GLASS in 1 CARTON (50242-201-01) / 1 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2025-12-19
Brand lunsumio velo
Generic mosunetuzumab
Sample Package No

Linked Drug Pages (1)

Lunsumio Velo ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "9f54a0a1-d24b-429e-9a1b-393ed834f1a6", "openfda": {"unii": ["LDJ89SS0YG"], "rxcui": ["2729433", "2729436", "2729439", "2729442"], "spl_set_id": ["6a2b6dc2-48bd-4da7-a611-bc6bae2893c8"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (50242-201-01)  / 1 mL in 1 VIAL, GLASS", "package_ndc": "50242-201-01", "marketing_start_date": "20251219"}], "brand_name": "Lunsumio Velo", "product_id": "50242-201_9f54a0a1-d24b-429e-9a1b-393ed834f1a6", "dosage_form": "INJECTION", "product_ndc": "50242-201", "generic_name": "Mosunetuzumab", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lunsumio Velo", "active_ingredients": [{"name": "MOSUNETUZUMAB", "strength": "45 mg/mL"}], "application_number": "BLA761263", "marketing_category": "BLA", "marketing_start_date": "20251219", "listing_expiration_date": "20261231"}