NDC 63323-649
Levothyroxine Sodium 100 ug per 5 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 100 ug per 5 mL
- Approval
- NDA NDA202231
- On the market since
- Jun 24, 2011
- Package NDCs
63323-649-07- Official label
- DailyMed (National Library of Medicine), updated Apr 17, 2025
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