NDC 21695-796
Amiodarone hydrochloride 200 mg tablet
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-227.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Amiodarone: every company that makes it
- Form
- tablet
- Strength
- 200 mg
- Approval
- ANDA ANDA079029
- On the market since
- Aug 10, 2009
- Package NDCs
21695-796-3021695-796-90- Official label
- DailyMed (National Library of Medicine), updated Apr 13, 2011
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