NDC 51672-4056
Amiodarone Hydrochloride 300 mg tablet
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Taro Pharmaceutical Industries Ltd. | Haifa Bay, Israel | Makes it | No problems foundDec 8, 2022 · 7 inspections |
Product details
- Generic drug
- Amiodarone: every company that makes it
- Form
- tablet, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA076362
- On the market since
- Dec 2, 2003
- Package NDCs
51672-4056-051672-4056-151672-4056-351672-4056-6- Official label
- DailyMed (National Library of Medicine), updated Mar 11, 2026
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