NDC 51662-1719
Furosemide 10 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-310.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aspiro Pharma Limited | Siddipet, India | Makes it | Problems found, fixed voluntarilyAug 11, 2023 · 1 inspection |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA217557
- On the market since
- Dec 13, 2024
- Package NDCs
51662-1719-151662-1719-251662-1719-3- Official label
- DailyMed (National Library of Medicine), updated Oct 19, 2026
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