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United States · US · US:50242-159_2800ba90-bfda-4932-9aae-9ef9166cd7e8

Lunsumio

UNIISPLATC L01FX25

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerGenentech, Inc.
CountryUS (United States)
ATC codeL01FX25
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5024215901
    1 VIAL in 1 CARTON (50242-159-01) / 1 mL in 1 VIAL

Annotations

UNII (FDA Substance ID)
LDJ89SS0YG
MOSUNETUZUMAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "LDJ89SS0YG",
    "rxcui": null,
    "inchikey": null,
    "display_name": "MOSUNETUZUMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "6a2b6dc2-48bd-4da7-a611-bc6bae2893c8": {
      "match": "brand_token",
      "title": "LUNSUMIO VELO (MOSUNETUZUMAB) INJECTION [GENENTECH, INC.]",
      "spl_version": "3",
      "published_date": "2025-12-24"
    }
  },
  "productid": "50242-159_2800ba90-bfda-4932-9aae-9ef9166cd7e8",
  "productndc": "50242-159",
  "dosage_form": "CONCENTRATE",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MOSUNETUZUMAB",
  "proprietary_name": "Lunsumio",
  "active_ingred_unit": "mg/mL",
  "application_number": "BLA761263",
  "marketing_category": "BLA",
  "nonproprietary_name": "Mosunetuzumab",
  "start_marketing_date": "20221222",
  "active_numerator_strength": "1"
}

Related drugs

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