Sevoflurane
Sevoflurane USPvolatile liquid for inhalation
Approved
Approval ID
5bfc1cef-824d-4ebf-bb4d-fbc46c0abb79
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 19, 2023
Manufacturers
FDA
Lannett Company, Inc.
DUNS: 002277481
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 Code0527-6123
Application NumberANDA214382
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sevoflurane
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateSeptember 19, 2023
FDA Product Classification
INGREDIENTS (1)
SevofluraneActive
Quantity: 250 mL in 250 mL
Code: 38LVP0K73A
Classification: ACTIB