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United States · US · US:61755-014_a8be5cf0-49ba-4795-a2e5-7ea07f495958

VEOPOZ

UNIISPLATC L04AJ11

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

Identification

ManufacturerRegeneron Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeL04AJ11
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6175501401
    1 VIAL, SINGLE-DOSE in 1 CARTON (61755-014-01) / 2 mL in 1 VIAL, SINGLE-DOSE (61755-014-00)

Annotations

UNII (FDA Substance ID)
0JJ21K6L2I
POZELIMAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "0JJ21K6L2I",
    "rxcui": null,
    "inchikey": null,
    "display_name": "POZELIMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS; SUBCUTANEOUS",
  "spl_meta": {
    "a8d6f10e-9430-450a-a3dd-b538f9b2a308": {
      "match": "brand_token",
      "title": "VEOPOZ (POZELIMAB) INJECTION, SOLUTION [REGENERON PHARMACEUTICALS, INC.]",
      "spl_version": "6",
      "published_date": "2025-12-10"
    }
  },
  "productid": "61755-014_a8be5cf0-49ba-4795-a2e5-7ea07f495958",
  "productndc": "61755-014",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "POZELIMAB",
  "proprietary_name": "VEOPOZ",
  "active_ingred_unit": "mg/mL",
  "application_number": "BLA761339",
  "marketing_category": "BLA",
  "nonproprietary_name": "Pozelimab",
  "start_marketing_date": "20230818",
  "active_numerator_strength": "200"
}

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