Sevoflurane
Sevoflurane USP volatile liquid for inhalation
Approved
Approval ID
c808afe1-ebf1-44cf-9187-09656331bff5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 12, 2024
Manufacturers
FDA
Shandong New Time Pharmaceutical Co., Ltd.
DUNS: 545298254
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 Code42677-308
Application NumberANDA214382
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sevoflurane
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJanuary 12, 2024
FDA Product Classification
INGREDIENTS (1)
SEVOFLURANEActive
Quantity: 250 mL in 250 mL
Code: 38LVP0K73A
Classification: ACTIB