NDC 0641-6008
Bumetanide 0.25 mg per 1 mL injection, solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's 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 |
Product details
- Generic drug
- Bumetanide: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 0.25 mg per 1 mL
- Approval
- ANDA ANDA079196
- On the market since
- Apr 30, 2008
- Package NDCs
0641-6008-010641-6008-10- Official label
- DailyMed (National Library of Medicine), updated Jul 8, 2026
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