Lupin Limited
Dhar, India · makes it and packages it
Problems found, fixed voluntarily Last FDA inspection Sep 27, 2024. 4 inspections on record.
NDC 51655-985
Levothyroxine Sodium 0.025 mg tablet
On the label: Northwind Pharmaceuticals.
It's a repackaged product: Northwind Pharmaceuticals rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-965.
Where the pills inside were made
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Dec 20, 2024 · Class II · Terminated
Failed Impurities/Degradation Specifications: Out of specifications result observed in the drug substance for impurity test during 3-month long term stability study.
Lots: Lot# LA01276, Exp Date: 07/2026
Product details
- Generic drug
- Levothyroxine: see every company that makes it
- Form
- tablet, oral
- Strength
- 0.025 mg
- Approval
- ANDA ANDA209713
- On the market since
- May 4, 2022
- Package NDCs
51655-985-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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