LANTIDRA

UNIISPLATC A10XX02

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

Identification

ManufacturerCellTrans Inc.

CountryUS (United States)

ATC codeA10XX02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7353900101
400 mL in 1 BAG (73539-001-01)

Annotations

UNII (FDA Substance ID)

FW00DG4E3P

DONISLECEL

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "FW00DG4E3P",
    "rxcui": null,
    "inchikey": null,
    "display_name": "DONISLECEL",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVASCULAR",
  "spl_meta": {
    "24610d9f-0c5a-4f55-93b3-d456300bfd5d": {
      "match": "brand_token",
      "title": "LANTIDRA (DONISLECEL) SOLUTION [CELLTRANS INC.]",
      "spl_version": "3",
      "published_date": "2026-01-15"
    }
  },
  "productid": "73539-001_a3163e14-0404-4e27-884b-f6f9f7f695bc",
  "productndc": "73539-001",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "CELLULAR THERAPY",
  "substance_name": "DONISLECEL",
  "proprietary_name": "LANTIDRA",
  "active_ingred_unit": "[arb'U]/400mL",
  "application_number": "BLA125734",
  "marketing_category": "BLA",
  "nonproprietary_name": "DONISLECEL",
  "start_marketing_date": "20230628",
  "active_numerator_strength": "5000"
}

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