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United States · US · US:0069-0502_39aa36a4-7b51-43af-9bf0-d812b3f9bd1d

XELJANZ

Orange BookUNIISPLATC L04AF01

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

Identification

ManufacturerPfizer Laboratories Div Pfizer Inc
CountryUS (United States)
ATC codeL04AF01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0069050230
    30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0502-30)

Annotations

UNII (FDA Substance ID)
O1FF4DIV0D
TOFACITINIB CITRATE
RxCUI 1358492
Orange Book
N208246
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "O1FF4DIV0D",
    "rxcui": "1358492",
    "inchikey": "SYIKUFDOYJFGBQ-YLAFAASESA-N",
    "display_name": "TOFACITINIB CITRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "68e3d6b2-7838-4d2d-a417-09d919b43e13": {
      "match": "brand_token",
      "title": "XELJANZ (TOFACITINIB) TABLET, FILM COATED XELJANZ XR (TOFACITINIB) TABLET, EXTENDED RELEASE XELJANZ (TOFACITINIB) SOLUTION [U.S. PHARMACEUTICALS]",
      "spl_version": "17",
      "published_date": "2026-03-30"
    }
  },
  "productid": "0069-0502_39aa36a4-7b51-43af-9bf0-d812b3f9bd1d",
  "productndc": "0069-0502",
  "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "208246",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 11MG BASE",
        "product_no": "001",
        "approval_date": "Feb 23, 2016"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 22MG BASE",
        "product_no": "002",
        "approval_date": "Dec 12, 2019"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "TOFACITINIB CITRATE",
  "proprietary_name": "XELJANZ",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA208246",
  "marketing_category": "NDA",
  "nonproprietary_name": "tofacitinib",
  "start_marketing_date": "20200121",
  "active_numerator_strength": "22"
}

Related drugs

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