Blenrep

UNIISPLATC L01FX15

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerGlaxoSmithKline LLC

CountryUS (United States)

ATC codeL01FX15

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0173091301
1 VIAL in 1 CARTON (0173-0913-01) / 1.4 mL in 1 VIAL

Annotations

UNII (FDA Substance ID)

DB1041CXDG

BELANTAMAB MAFODOTIN

RxCUI 2387834

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "DB1041CXDG",
    "rxcui": "2387834",
    "inchikey": null,
    "display_name": "BELANTAMAB MAFODOTIN",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "aef7c34c-fef8-407c-99c0-a68aded53c60": {
      "match": "brand_token",
      "title": "BLENREP (BELANTAMAB MAFODOTIN) INJECTION, POWDER, FOR SOLUTION [GLAXOSMITHKLINE LLC]",
      "spl_version": "1",
      "published_date": "2025-11-17"
    }
  },
  "productid": "0173-0913_aef7c34c-fef8-407c-99c0-a68aded53c60",
  "productndc": "0173-0913",
  "dosage_form": "INJECTION, POWDER, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BELANTAMAB MAFODOTIN",
  "proprietary_name": "Blenrep",
  "active_ingred_unit": "mg/mL",
  "application_number": "BLA761440",
  "marketing_category": "BLA",
  "nonproprietary_name": "belantamab mafodotin",
  "start_marketing_date": "20251023",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code L01FX15.

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