Ultane
ULTANE (sevoflurane) volatile liquid for inhalation
Approved
Approval ID
4c6e76bc-c964-4955-e0a3-511d3386a9cc
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 18, 2022
Manufacturers
FDA
AbbVie Inc.
DUNS: 078458370
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sevoflurane
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0074-4456
Application NumberNDA020478
Product Classification
M
Marketing Category
C73594
G
Generic Name
Sevoflurane
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateAugust 30, 2022
FDA Product Classification
INGREDIENTS (1)
SEVOFLURANEActive
Quantity: 250 mL in 250 mL
Code: 38LVP0K73A
Classification: ACTIB