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United States · US · US:57962-420_43280dcb-52ae-40e4-bd52-723f71f74ab7

Imbruvica

Orange BookUNIISPLATC L01EL01

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

Identification

ManufacturerPharmacyclics LLC
CountryUS (United States)
ATC codeL01EL01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5796242028
    1 BLISTER PACK in 1 CARTON (57962-420-28) / 28 TABLET, FILM COATED in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
1X70OSD4VX
IBRUTINIB
RxCUI 1442981
Orange Book
N210563
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "1X70OSD4VX",
    "rxcui": "1442981",
    "inchikey": "XYFPWWZEPKGCCK-GOSISDBHSA-N",
    "display_name": "IBRUTINIB",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "0dfd0279-ff17-4ea9-89be-9803c71bab44": {
      "match": "brand_token",
      "title": "IMBRUVICA (IBRUTINIB) CAPSULE IMBRUVICA (IBRUTINIB) TABLET, FILM COATED IMBRUVICA (IBRUTINIB) SUSPENSION [PHARMACYCLICS LLC]",
      "spl_version": "65",
      "published_date": "2026-01-08"
    }
  },
  "productid": "57962-420_43280dcb-52ae-40e4-bd52-723f71f74ab7",
  "productndc": "57962-420",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "210563",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "140MG",
        "product_no": "001",
        "approval_date": "Feb 16, 2018"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "280MG",
        "product_no": "002",
        "approval_date": "Feb 16, 2018"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "420MG",
        "product_no": "003",
        "approval_date": "Feb 16, 2018"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "560MG",
        "product_no": "004",
        "approval_date": "Feb 16, 2018"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "IBRUTINIB",
  "proprietary_name": "Imbruvica",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA210563",
  "marketing_category": "NDA",
  "nonproprietary_name": "Ibrutinib",
  "start_marketing_date": "20180216",
  "active_numerator_strength": "420"
}

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