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United States · US · US:10122-620_8c5e6180-c346-48e7-818d-471089de4ee7

KENGREAL

Orange BookUNIISPLATC B01AC25

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

Identification

ManufacturerChiesi USA, Inc.
CountryUS (United States)
ATC codeB01AC25
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    1012262010
    10 VIAL, SINGLE-USE in 1 CARTON (10122-620-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (10122-620-01)

Annotations

UNII (FDA Substance ID)
6AQ1Y404U7
CANGRELOR
RxCUI 1656052
Orange Book
N204958
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "6AQ1Y404U7",
    "rxcui": "1656052",
    "inchikey": "PAEBIVWUMLRPSK-IDTAVKCVSA-N",
    "display_name": "CANGRELOR",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "88b434fa-8891-4fd5-9d86-7ea64667c08f": {
      "match": "brand_token",
      "title": "KENGREAL (CANGRELOR) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [CHIESI USA, INC.]",
      "spl_version": "10",
      "published_date": "2025-11-17"
    }
  },
  "productid": "10122-620_8c5e6180-c346-48e7-818d-471089de4ee7",
  "productndc": "10122-620",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "orange_book": {
    "appl_no": "204958",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AP",
        "strength": "50MG/VIAL",
        "product_no": "001",
        "approval_date": "Jun 22, 2015"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CANGRELOR",
  "proprietary_name": "KENGREAL",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA204958",
  "marketing_category": "NDA",
  "nonproprietary_name": "cangrelor",
  "start_marketing_date": "20150708",
  "active_numerator_strength": "50"
}

Related drugs

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