NDC 53217-271
Furosemide 20 mg tablet
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC 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 |
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
- Strength
- 20 mg
- Approval
- ANDA ANDA077293
- On the market since
- Feb 1, 2006
- Package NDCs
53217-271-0053217-271-0853217-271-1453217-271-2053217-271-3053217-271-6053217-271-90- Official label
- DailyMed (National Library of Medicine), updated Apr 7, 2017
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