NDC 70518-3757
Furosemide 20 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
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
- Jun 11, 2023
- Package NDCs
70518-3757-070518-3757-170518-3757-2- Official label
- DailyMed (National Library of Medicine), updated Aug 17, 2026
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