NDC 51662-1449
Bumetanide 0.25 mg per 1 mL injection
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0641-6008.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Pharmaceuticals USA Inc. | Cherry Hill, NJ, United States | Makes it, tests it and labels it | No problems foundMay 13, 2026 · 18 inspections |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Bumetanide: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 0.25 mg per 1 mL
- Approval
- ANDA ANDA079196
- On the market since
- Jan 11, 2020
- Package NDCs
51662-1449-1- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2025
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