NDC 71288-203
Furosemide 10 mg per 1 mL injection, solution
On the label: Meitheal Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd (API and FDF Site) | Nanjing, China | Makes it | Problems found, fixed voluntarilyNov 10, 2023 · 3 inspections |
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA212803
- On the market since
- Jan 27, 2022
- Package NDCs
71288-203-0271288-203-0371288-203-0471288-203-0571288-203-1071288-203-11- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2026
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