NDC 69315-701
Ethacrynate Sodium 50 mg per 50 mL injection, powder, lyophilized, for solution
On the label: Leading Pharma, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bioindustria Laboratorio Italiano Medicinali S.p.A | Novi Ligure, Italy | Makes it and tests it | Problems found, fixed voluntarilyJul 25, 2025 · 5 inspections |
Product details
- Generic drug
- Ethacrynic Acid: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 50 mg per 50 mL
- Approval
- ANDA ANDA208663
- On the market since
- Jan 9, 2026
- Package NDCs
69315-701-50- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2026
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