NDC 0404-9864
Furosemide 20 mg per 2 mL injection, solution
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from AuroMedics Pharma LLC's NDC 55150-322.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 20 mg per 2 mL
- Approval
- ANDA ANDA212174
- On the market since
- Jan 10, 2022
- Package NDCs
0404-9864-02- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2026
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