NDC 63323-885
Levothyroxine Sodium 20 ug per 1 mL injection, 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, solution, intravenous
- Strength
- 20 ug per 1 mL
- Approval
- NDA NDA210632
- On the market since
- May 29, 2018
- Package NDCs
63323-885-10- Official label
- DailyMed (National Library of Medicine), updated Mar 17, 2025
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