NDC 70518-1939
Amiodarone Hydrochloride 200 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-732.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Amiodarone: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA204742
- On the market since
- Mar 6, 2019
- Package NDCs
70518-1939-070518-1939-1- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2026
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