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United States · US · US:79952-110_42deedca-b1fa-45ec-aea7-69ce6ecb8c96

ZYNLONTA

UNIISPLATC L01FX22

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

Identification

ManufacturerADC Therapeutics America, Inc.
CountryUS (United States)
ATC codeL01FX22
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7995211001
    1 VIAL, SINGLE-DOSE in 1 CARTON (79952-110-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Annotations

UNII (FDA Substance ID)
7K5O7P6QIU
LONCASTUXIMAB TESIRINE
RxCUI 2540964
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7K5O7P6QIU",
    "rxcui": "2540964",
    "inchikey": null,
    "display_name": "LONCASTUXIMAB TESIRINE",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "af54af12-3edf-4301-8bc5-0446bc813c1d": {
      "match": "brand_token",
      "title": "ZYNLONTA (LONCASTUXIMAB TESIRINE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ADC THERAPEUTICS AMERICA, INC.]",
      "spl_version": "14",
      "published_date": "2026-03-02"
    }
  },
  "productid": "79952-110_42deedca-b1fa-45ec-aea7-69ce6ecb8c96",
  "productndc": "79952-110",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LONCASTUXIMAB TESIRINE",
  "proprietary_name": "ZYNLONTA",
  "active_ingred_unit": "mg/2mL",
  "application_number": "BLA761196",
  "marketing_category": "BLA",
  "nonproprietary_name": "loncastuximab tesirine",
  "start_marketing_date": "20210430",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code L01FX22.

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