Sevoflurane
Sevoflurane, USP Volatile Liquid for Inhalation
Approved
Approval ID
06b9f724-6425-4976-93eb-b9ca343ef5cf
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 29, 2024
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
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 Code72162-2245
Application NumberANDA077867
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sevoflurane
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJanuary 29, 2024
FDA Product Classification
INGREDIENTS (1)
SEVOFLURANEActive
Quantity: 1 mL in 1 mL
Code: 38LVP0K73A
Classification: ACTIB