NDC 72673-072
Amiodarone Hydrochloride 50 mg per 1 mL injection, solution
On the label: Zhejiang Poly Pharm. Co., Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zhejiang Poly Pharm. Co., Ltd | Hangzhou, China | Makes it | Problems found, fixed voluntarilyNov 8, 2024 · 1 inspection |
Product details
- Generic drug
- Amiodarone: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA218253
- On the market since
- Feb 6, 2023
- Package NDCs
72673-072-10- Official label
- DailyMed (National Library of Medicine), updated Jan 16, 2026
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