NDC 51655-269
Furosemide 20 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Leading Pharma, LLC's NDC 69315-116.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Leading Pharma, LLC | Fairfield, NJ, United States | Makes it | Problems found, fixed voluntarilyOct 21, 2024 · 13 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Mar 20, 2026 · Class II · Leading Pharma, LLC
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
Lots: Lots# H03125, H03225, H03325, Exp Date: 2027/08
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA077293
- On the market since
- Aug 8, 2022
- Package NDCs
51655-269-2551655-269-2651655-269-5251655-269-53- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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