Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Shirley, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 24, 2024 · 12 inspections, 1 with FDA action |
Recalls
- Jul 24, 2026 · Class II · American Regent, Inc.
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Lots: Lot #: 25090, Exp. Date 2/28/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Selenium: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 6 ug per 1 mL
- Approval
- NDA NDA209379
- On the market since
- Mar 28, 2022
- Package NDCs
0517-6502-010517-6502-10- Official label
- DailyMed (National Library of Medicine), updated Aug 1, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?