EMRELIS

UNIISPL

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

Identification

ManufacturerAbbVie Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0074104401
1 VIAL, SINGLE-DOSE in 1 CARTON (0074-1044-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Annotations

UNII (FDA Substance ID)

976X9VXC3Z

TELISOTUZUMAB VEDOTIN

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "976X9VXC3Z",
    "rxcui": null,
    "inchikey": null,
    "display_name": "TELISOTUZUMAB VEDOTIN",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "bc04f980-3957-4e35-ab81-8ec2ffe87215": {
      "match": "brand_token",
      "title": "EMRELIS (TELISOTUZUMAB VEDOTIN) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ABBVIE INC.]",
      "spl_version": "3",
      "published_date": "2025-07-10"
    }
  },
  "productid": "0074-1044_998985bb-7cd1-4e80-bd08-8fc7c503f982",
  "productndc": "0074-1044",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "TELISOTUZUMAB VEDOTIN",
  "proprietary_name": "EMRELIS",
  "active_ingred_unit": "mg/mL",
  "application_number": "BLA761384",
  "marketing_category": "BLA",
  "nonproprietary_name": "Telisotuzumab Vedotin",
  "start_marketing_date": "20250514",
  "active_numerator_strength": "20"
}

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