NDC 70518-4679
Furosemide 20 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ipca Laboratories Limited's NDC 83980-002.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Guardian Drug Company, Inc. | Dayton, NJ, United States | Makes it | No problems foundJan 16, 2026 · 9 inspections |
| Ipca Laboratories Limited | Silvassa, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 26, 2023 · 5 inspections, 2 with FDA action |
| Ipca Laboratories Limited | Dhar, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 23, 2023 · 4 inspections, 1 with FDA action |
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078010
- On the market since
- Jun 22, 2026
- Package NDCs
70518-4679-0- Official label
- DailyMed (National Library of Medicine), updated Jun 23, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?