lunsumio

Generic: mosunetuzumab

Labeler: genentech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name lunsumio
Generic Name mosunetuzumab
Labeler genentech, inc.
Dosage Form CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

mosunetuzumab 30 mg/30mL

Manufacturer
Genentech, Inc.

Identifiers & Regulatory

Product NDC 50242-142
Product ID 50242-142_2800ba90-bfda-4932-9aae-9ef9166cd7e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA761263
Listing Expiration 2026-12-31
Marketing Start 2022-12-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50242142
Hyphenated Format 50242-142

Supplemental Identifiers

RxCUI
2625129 2625135 2625137 2625138
UNII
LDJ89SS0YG

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lunsumio (source: ndc)
Generic Name mosunetuzumab (source: ndc)
Application Number BLA761263 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 30 mg/30mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (50242-142-01) / 30 mL in 1 VIAL
source: ndc

Packages (1)

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

Ingredients (1)

mosunetuzumab (30 mg/30mL)

Linked Drug Pages (1)

Lunsumio ndc-match (0.9)

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"}