Suprane
These highlights do not include all the information needed to use Suprane (desflurane, USP) safely and effectively. See full prescribing information for Suprane (desflurane, USP).Suprane (desflurane, USP) Volatile Liquid for InhalationInitial U.S. Approval: 1992
Approved
Approval ID
a3e4c8e5-bff0-4a8f-8401-e9866c846ee2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 16, 2023
Manufacturers
FDA
Henry Schein, Inc.
DUNS: 012430880
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Desflurane
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0404-9961
Application NumberNDA020118
Product Classification
M
Marketing Category
C73594
G
Generic Name
Desflurane
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateNovember 16, 2023
FDA Product Classification
INGREDIENTS (1)
DesfluraneActive
Quantity: 240 mL in 240 mL
Code: CRS35BZ94Q
Classification: ACTIB