SOLIRIS

UNIISPLATC L04AJ01

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

Identification

ManufacturerAlexion Pharmaceuticals Inc.

CountryUS (United States)

ATC codeL04AJ01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
2568200101
1 VIAL in 1 CARTON (25682-001-01) / 30 mL in 1 VIAL

Annotations

UNII (FDA Substance ID)

A3ULP0F556

ECULIZUMAB

RxCUI 591781

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "A3ULP0F556",
    "rxcui": "591781",
    "inchikey": null,
    "display_name": "ECULIZUMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "ebcd67fa-b4d1-4a22-b33d-ee8bf6b9c722": {
      "match": "brand_token",
      "title": "SOLIRIS (ECULIZUMAB) INJECTION, SOLUTION, CONCENTRATE [ALEXION PHARMACEUTICALS INC.]",
      "spl_version": "42",
      "published_date": "2025-03-11"
    }
  },
  "productid": "25682-001_25021c88-95e1-42f0-b895-921526b90642",
  "productndc": "25682-001",
  "dosage_form": "INJECTION, SOLUTION, CONCENTRATE",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ECULIZUMAB",
  "proprietary_name": "SOLIRIS",
  "active_ingred_unit": "mg/30mL",
  "application_number": "BLA125166",
  "marketing_category": "BLA",
  "nonproprietary_name": "ECULIZUMAB",
  "start_marketing_date": "20070402",
  "active_numerator_strength": "300"
}

Related drugs

Other records sharing ATC code L04AJ01.

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