NDC 82868-050
Furosemide 20 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-562.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Graviti Pharmaceuticals Private Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilyJul 28, 2026 · 2 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Jan 10, 2026 · Class II · Graviti Pharmaceuticals Private Limited
Presence of Foreign Substance
Lots: Lot# FUB125042G; Exp. 05/13/2027
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 ANDA216629
- On the market since
- Feb 29, 2024
- Package NDCs
82868-050-3082868-050-90- Official label
- DailyMed (National Library of Medicine), updated Jan 2, 2026
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