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United States · US · US:0003-3734_645d02cf-536a-4ceb-b812-660735b38e92

OPDIVO

UNIISPLATC L01FF01

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

Identification

ManufacturerE.R. Squibb & Sons, L.L.C.
CountryUS (United States)
ATC codeL01FF01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0003373413
    1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3734-13) / 24 mL in 1 VIAL, SINGLE-DOSE

Annotations

UNII (FDA Substance ID)
31YO63LBSN
NIVOLUMAB
RxCUI 1597876
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "31YO63LBSN",
    "rxcui": "1597876",
    "inchikey": null,
    "display_name": "NIVOLUMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "7f8c38fa-42f4-4387-9e8c-7a1c66855d8b": {
      "match": "brand_token",
      "title": "OPDIVO QVANTIG (NIVOLUMAB AND HYALURONIDASE-NVHY) INJECTION, SOLUTION [E.R. SQUIBB & SONS, L.L.C.]",
      "spl_version": "8",
      "published_date": "2026-05-28"
    }
  },
  "productid": "0003-3734_645d02cf-536a-4ceb-b812-660735b38e92",
  "productndc": "0003-3734",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NIVOLUMAB",
  "proprietary_name": "OPDIVO",
  "active_ingred_unit": "mg/mL",
  "application_number": "BLA125554",
  "marketing_category": "BLA",
  "nonproprietary_name": "nivolumab",
  "start_marketing_date": "20171208",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code L01FF01.

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