OPDUALAG

UNIISPLATC L01FF

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

Identification

ManufacturerE.R. Squibb & Sons, L.L.C.

CountryUS (United States)

ATC codeL01FF

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0003712511
1 VIAL, SINGLE-DOSE in 1 CARTON (0003-7125-11) / 20 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": {
    "b22c9d83-3256-4e17-85f7-f331a504adc6": {
      "match": "brand_token",
      "title": "OPDUALAG (NIVOLUMAB AND RELATLIMAB-RMBW) INJECTION [E.R. SQUIBB & SONS, L.L.C.]",
      "spl_version": "2",
      "published_date": "2024-03-07"
    }
  },
  "productid": "0003-7125_1150d07b-4d33-4285-a242-1ecf12ed5a4c",
  "productndc": "0003-7125",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NIVOLUMAB; RELATLIMAB",
  "proprietary_name": "OPDUALAG",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "BLA761234",
  "marketing_category": "BLA",
  "nonproprietary_name": "nivolumab and relatlimab-rmbw",
  "start_marketing_date": "20220318",
  "active_numerator_strength": "12; 4"
}

Related drugs

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