NDC 70511-113
Levothyroxine Sodium 500 ug per 5 mL injection, powder, lyophilized, for solution
On the label: MAIA Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it | Problems found, fixed voluntarilyJul 25, 2024 · 7 inspections |
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 ug per 5 mL
- Approval
- ANDA ANDA208749
- On the market since
- Dec 27, 2018
- Package NDCs
70511-113-10- Official label
- DailyMed (National Library of Medicine), updated Aug 5, 2026
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