Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
| PPD Development, L.P. | Middleton, WI, United States | Tests it | Problems found, fixed voluntarilySep 25, 2025 · 6 inspections |
Product details
- Generic drug
- Manganese Cation (2+): every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.1 mg per 1 mL
- Approval
- NDA NDA018962
- On the market since
- Jan 31, 2005
- Package NDCs
0409-4091-010409-4091-11- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2026
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