Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Hilliard, OH, United States | Makes it | Problems found, fixed voluntarilyJun 18, 2026 · 8 inspections |
| American Regent, Inc. | Shirley, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 24, 2024 · 12 inspections, 1 with FDA action |
| Vifor (International) Inc. | St. Gallen, Switzerland | Makes it and makes the active ingredient | Problems found, fixed voluntarilySep 6, 2024 · 4 inspections |
| American Regent, Inc. | Columbus, OH, United States | Tests it | Problems found, fixed voluntarilyMar 5, 2026 · 8 inspections |
Recalls
- Nov 11, 2024 · Class II · American Regent, Inc.
Presence of Particulate Matter: Potential for glass delamination from the vials.
Lots: Lot #s: 4205, Exp 05/31/2026; 24229, 24233, 24239, Exp 07/31/2026.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ferric Cation: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 20 mg per 1 mL
- Approval
- NDA NDA021135
- On the market since
- Jan 27, 2011
- Package NDCs
0517-2325-010517-2325-10- Official label
- DailyMed (National Library of Medicine), updated Mar 1, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?