NDC 70518-4444
Furosemide 10 mg per 1 mL injection, solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Baxter Healthcare Corporation's NDC 36000-283.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxter Pharmaceuticals India Private Limited | Ahmedabad, India | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionJan 27, 2023 · 9 inspections, 3 with FDA action |
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA202747
- On the market since
- Aug 15, 2025
- Package NDCs
70518-4444-070518-4444-1- Official label
- DailyMed (National Library of Medicine), updated Sep 11, 2026
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