Package 50242-142-01

Brand: lunsumio

Generic: mosunetuzumab
NDC Package

Package Facts

Identity

Package NDC 50242-142-01
Digits Only 5024214201
Product NDC 50242-142
Product ID 50242-142_2800ba90-bfda-4932-9aae-9ef9166cd7e8
Description

1 VIAL in 1 CARTON (50242-142-01) / 30 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-12-22
Brand lunsumio
Generic mosunetuzumab
Sample Package No

Linked Drug Pages (1)

Lunsumio ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2800ba90-bfda-4932-9aae-9ef9166cd7e8", "openfda": {"unii": ["LDJ89SS0YG"], "rxcui": ["2625129", "2625135", "2625137", "2625138"], "spl_set_id": ["2ef0cf38-101c-4681-98fe-c05dc9ead443"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (50242-142-01)  / 30 mL in 1 VIAL", "package_ndc": "50242-142-01", "marketing_start_date": "20221222"}], "brand_name": "Lunsumio", "product_id": "50242-142_2800ba90-bfda-4932-9aae-9ef9166cd7e8", "dosage_form": "CONCENTRATE", "product_ndc": "50242-142", "generic_name": "Mosunetuzumab", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lunsumio", "active_ingredients": [{"name": "MOSUNETUZUMAB", "strength": "30 mg/30mL"}], "application_number": "BLA761263", "marketing_category": "BLA", "marketing_start_date": "20221222", "listing_expiration_date": "20261231"}