NDC 70771-1818
Levothyroxine Sodium 100 ug per 5 mL injection, powder, lyophilized, for solution
On the label: Cadila Healthcare Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Vadodara, India | Makes it and tests it | Serious problems, FDA actionApr 23, 2024 · 2 inspections, 1 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
- ANDA ANDA217066
- On the market since
- Nov 1, 2024
- Package NDCs
70771-1818-1- Official label
- DailyMed (National Library of Medicine), updated Oct 24, 2024
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