Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxter Healthcare Corporation | Guayama, PR, United States | Makes it, makes the active ingredient, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 26, 2025 · 8 inspections, 1 with FDA action |
Recalls
- Jun 13, 2019 · Class II · Baxter Healthcare Corporation
Failed Stability Specifications
Lots: Lot #: S110F822 Exp. 5/31/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sevoflurane: every company that makes it
- Form
- liquid, respiratory (inhalation)
- Strength
- 250 mL per 250 mL
- Approval
- ANDA ANDA075895
- On the market since
- Jul 2, 2002
- Package NDCs
10019-651-64- Official label
- DailyMed (National Library of Medicine), updated Mar 28, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?