Kineret

UNIISPLATC L04AC03

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

Identification

ManufacturerSwedish Orphan Biovitrum AB (publ)

CountryUS (United States)

ATC codeL04AC03

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
6665823407
7 SYRINGE, GLASS in 1 CARTON (66658-234-07) / .67 mL in 1 SYRINGE, GLASS
ndc11
6665823428
4 CARTON in 1 CASE (66658-234-28) / 7 SYRINGE, GLASS in 1 CARTON / .67 mL in 1 SYRINGE, GLASS

Annotations

UNII (FDA Substance ID)

9013DUQ28K

ANAKINRA

RxCUI 72435

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "9013DUQ28K",
    "rxcui": "72435",
    "inchikey": null,
    "display_name": "ANAKINRA",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBCUTANEOUS",
  "spl_meta": {
    "d9d74915-6606-4570-9c52-c4001d3177de": {
      "match": "brand_token",
      "title": "KINERET (ANAKINRA) INJECTION, SOLUTION [SWEDISH ORPHAN BIOVITRUM AB (PUBL)]",
      "spl_version": "24",
      "published_date": "2026-04-10"
    }
  },
  "productid": "66658-234_d1acb9d5-9241-4aeb-b3e7-f05dbc8c15a2",
  "productndc": "66658-234",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ANAKINRA",
  "proprietary_name": "Kineret",
  "active_ingred_unit": "mg/.67mL",
  "application_number": "BLA103950",
  "marketing_category": "BLA",
  "nonproprietary_name": "anakinra",
  "start_marketing_date": "20091215",
  "active_numerator_strength": "100"
}

Related drugs

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