NDC 50090-7705
Furosemide 40 mg tablet
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Ipca Laboratories Limited's NDC 83980-003.
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 |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- tablet, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA078010
- On the market since
- Jun 3, 2024
- Package NDCs
50090-7705-0- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2025
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