MedPath

Isoflurane

Isoflurane, USP Liquid For Inhalation

Approved
Approval ID

e8e57cd7-b662-4e1c-beda-e73a4b3d16ae

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Mar 27, 2020

Manufacturers
FDA

Halocarbon Life Sciences, LLC

DUNS: 002027514

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Isoflurane

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code12164-012
Application NumberANDA075225
Product Classification
M
Marketing Category
C73584
G
Generic Name
Isoflurane
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateMarch 27, 2020
FDA Product Classification

INGREDIENTS (1)

IsofluraneActive
Quantity: 1 mL in 1 mL
Code: CYS9AKD70P
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Isoflurane - FDA Drug Approval Details