ultane
Generic: sevoflurane
Labeler: abbvie inc.Drug Facts
Product Profile
Brand Name
ultane
Generic Name
sevoflurane
Labeler
abbvie inc.
Dosage Form
LIQUID
Routes
Active Ingredients
sevoflurane 250 mL/250mL
Manufacturer
Identifiers & Regulatory
Product NDC
0074-4456
Product ID
0074-4456_20a177a4-8440-46f9-98f4-c51d395e4a46
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020478
Listing Expiration
2026-12-31
Marketing Start
1995-06-07
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00744456
Hyphenated Format
0074-4456
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ultane (source: ndc)
Generic Name
sevoflurane (source: ndc)
Application Number
NDA020478 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mL/250mL
Packaging
- 250 mL in 1 BOTTLE, PLASTIC (0074-4456-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "20a177a4-8440-46f9-98f4-c51d395e4a46", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["38LVP0K73A"], "rxcui": ["200243", "541963"], "spl_set_id": ["4c6e76bc-c964-4955-e0a3-511d3386a9cc"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["AbbVie Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BOTTLE, PLASTIC (0074-4456-04)", "package_ndc": "0074-4456-04", "marketing_start_date": "19950607"}], "brand_name": "Ultane", "product_id": "0074-4456_20a177a4-8440-46f9-98f4-c51d395e4a46", "dosage_form": "LIQUID", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0074-4456", "generic_name": "Sevoflurane", "labeler_name": "AbbVie Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ultane", "active_ingredients": [{"name": "SEVOFLURANE", "strength": "250 mL/250mL"}], "application_number": "NDA020478", "marketing_category": "NDA", "marketing_start_date": "19950607", "listing_expiration_date": "20261231"}