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United States · US · US:51144-050_a695c1a2-3acc-468b-a829-c8761dc041f6

ADCETRIS

UNIISPLATC L01FX05

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

Identification

ManufacturerSEAGEN INC.
CountryUS (United States)
ATC codeL01FX05
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5114405001
    1 VIAL, SINGLE-DOSE in 1 BOX (51144-050-01) / 10.5 mL in 1 VIAL, SINGLE-DOSE

Annotations

UNII (FDA Substance ID)
7XL5ISS668
BRENTUXIMAB VEDOTIN
RxCUI 1147320
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7XL5ISS668",
    "rxcui": "1147320",
    "inchikey": null,
    "display_name": "BRENTUXIMAB VEDOTIN",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "3904f8dd-1aef-3490-e48f-bd55f32ed67f": {
      "match": "brand_token",
      "title": "ADCETRIS (BRENTUXIMAB VEDOTIN) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SEAGEN INC.]",
      "spl_version": "38",
      "published_date": "2025-11-17"
    }
  },
  "productid": "51144-050_a695c1a2-3acc-468b-a829-c8761dc041f6",
  "productndc": "51144-050",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BRENTUXIMAB VEDOTIN",
  "proprietary_name": "ADCETRIS",
  "active_ingred_unit": "mg/10.5mL",
  "application_number": "BLA125388",
  "marketing_category": "BLA",
  "nonproprietary_name": "brentuximab vedotin",
  "start_marketing_date": "20110825",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code L01FX05.

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