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United States · US · US:73207-101_142c8672-a552-4d20-9226-2a92aa9773d1

QINLOCK

Orange BookUNIISPLATC L01EX19

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

Identification

ManufacturerDeciphera Pharmaceuticals, LLC
CountryUS (United States)
ATC codeL01EX19
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    7320710130
    1 BOTTLE in 1 CARTON (73207-101-30) / 90 TABLET in 1 BOTTLE
  • ndc11
    7320710131
    1 BOTTLE in 1 CARTON (73207-101-31) / 30 TABLET in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
9XW757O13D
RIPRETINIB
RxCUI 2369389
Orange Book
N213973
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "9XW757O13D",
    "rxcui": "2369389",
    "inchikey": "CEFJVGZHQAGLHS-UHFFFAOYSA-N",
    "display_name": "RIPRETINIB",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9f18e462-03dd-4296-a02a-a0577e3ee78d": {
      "match": "brand_token",
      "title": "QINLOCK (RIPRETINIB) TABLET [DECIPHERA PHARMACEUTICALS, LLC\n]",
      "spl_version": "9",
      "published_date": "2025-05-14"
    }
  },
  "productid": "73207-101_142c8672-a552-4d20-9226-2a92aa9773d1",
  "productndc": "73207-101",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "213973",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "May 15, 2020"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "RIPRETINIB",
  "proprietary_name": "QINLOCK",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA213973",
  "marketing_category": "NDA",
  "nonproprietary_name": "Ripretinib",
  "start_marketing_date": "20200515",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code L01EX19.

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