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United States · US · US:49401-102_379d7f58-8f17-44b3-8336-6fe8ef015aed

BENLYSTA

UNIISPLATC L04AG04

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

Identification

ManufacturerGlaxoSmithKline LLC
CountryUS (United States)
ATC codeL04AG04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    4940110201
    1 VIAL in 1 CARTON (49401-102-01) / 5 mL in 1 VIAL

Annotations

UNII (FDA Substance ID)
73B0K5S26A
BELIMUMAB
RxCUI 1092437
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "73B0K5S26A",
    "rxcui": "1092437",
    "inchikey": null,
    "display_name": "BELIMUMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "2fa3c528-1777-4628-8a55-a69dae2381a3": {
      "match": "brand_token",
      "title": "BENLYSTA (BELIMUMAB) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION BENLYSTA (BELIMUMAB) SOLUTION [GLAXOSMITHKLINE LLC]",
      "spl_version": "37",
      "published_date": "2026-02-23"
    }
  },
  "productid": "49401-102_379d7f58-8f17-44b3-8336-6fe8ef015aed",
  "productndc": "49401-102",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BELIMUMAB",
  "proprietary_name": "BENLYSTA",
  "active_ingred_unit": "mg/5mL",
  "application_number": "BLA125370",
  "marketing_category": "BLA",
  "nonproprietary_name": "belimumab",
  "start_marketing_date": "20110310",
  "active_numerator_strength": "400"
}

Related drugs

Other records sharing ATC code L04AG04.

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