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United States · US · US:47335-237_294580cb-5622-4f48-89a8-99000a7a2964

ambrisentan

Orange BookUNIISPLATC C02KX02

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

Identification

ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeC02KX02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    4733523764
    3 BLISTER PACK in 1 CARTON (47335-237-64) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-237-60)
  • ndc11
    4733523766
    1 BLISTER PACK in 1 CARTON (47335-237-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-237-60)
  • ndc11
    4733523783
    30 TABLET, FILM COATED in 1 BOTTLE (47335-237-83)
  • ndc11
    4733523785
    10 TABLET, FILM COATED in 1 BOTTLE (47335-237-85)

Annotations

UNII (FDA Substance ID)
HW6NV07QEC
AMBRISENTAN
RxCUI 358274
Orange Book
A210784
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "HW6NV07QEC",
    "rxcui": "358274",
    "inchikey": "OUJTZYPIHDYQMC-LJQANCHMSA-N",
    "display_name": "AMBRISENTAN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "32549c43-f8ff-422c-b42d-ca0877e661cf": {
      "match": "brand_token",
      "title": "AMBRISENTAN TABLET, FILM COATED [ACTAVIS PHARMA, INC.]",
      "spl_version": "19",
      "published_date": "2026-04-09"
    }
  },
  "productid": "47335-237_294580cb-5622-4f48-89a8-99000a7a2964",
  "productndc": "47335-237",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "210784",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Mar 28, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Mar 28, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "AMBRISENTAN",
  "proprietary_name": "ambrisentan",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA210784",
  "marketing_category": "ANDA",
  "nonproprietary_name": "ambrisentan",
  "start_marketing_date": "20190429",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code C02KX02.

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