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United States · US · US:0074-4456_20a177a4-8440-46f9-98f4-c51d395e4a46

Ultane

Orange BookUNIISPLATC N01AB08

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

Identification

ManufacturerAbbVie Inc.
CountryUS (United States)
ATC codeN01AB08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0074445604
    250 mL in 1 BOTTLE, PLASTIC (0074-4456-04)

Annotations

UNII (FDA Substance ID)
38LVP0K73A
SEVOFLURANE
RxCUI 36453
Orange Book
N020478
AN
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "38LVP0K73A",
    "rxcui": "36453",
    "inchikey": "DFEYYRMXOJXZRJ-UHFFFAOYSA-N",
    "display_name": "SEVOFLURANE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "RESPIRATORY (INHALATION)",
  "spl_meta": {
    "c9aa6489-5a36-44ed-9512-b996833d82f7": {
      "match": "brand_token",
      "title": "ULTANE (SEVOFLURANE) LIQUID [ABBVIE INC.]",
      "spl_version": "1458",
      "published_date": "2025-02-24"
    }
  },
  "productid": "0074-4456_20a177a4-8440-46f9-98f4-c51d395e4a46",
  "productndc": "0074-4456",
  "dosage_form": "LIQUID",
  "orange_book": {
    "appl_no": "020478",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AN",
        "strength": "100%",
        "product_no": "001",
        "approval_date": "Jun 7, 1995"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SEVOFLURANE",
  "proprietary_name": "Ultane",
  "active_ingred_unit": "mL/250mL",
  "application_number": "NDA020478",
  "marketing_category": "NDA",
  "nonproprietary_name": "Sevoflurane",
  "start_marketing_date": "19950607",
  "active_numerator_strength": "250"
}

Related drugs

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