NDC 51655-604
Levothyroxine Sodium 112 ug tablet
On the label: Northwind Pharmaceuticals. It's repackaged from NDC 0378-1811, made by Mylan Pharmaceuticals Inc. (Levothyroxine Sodium). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Northwind Pharmaceuticals names for other drugs.
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- tablet, oral
- Strength
- 112 ug
- Approval
- ANDA ANDA076187
- On the market since
- Feb 18, 2021
- Package NDCs
51655-604-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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