NDC 53808-1066
Amiodarone hydrochloride 200 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy 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 |
Repackaging site
- State of Florida DOH Central Pharmacy, Location not on file · repackages it
Product details
- Generic drug
- Amiodarone: every company that makes it
- Form
- tablet
- Strength
- 200 mg
- Approval
- ANDA ANDA079029
- On the market since
- Nov 1, 2014
- Package NDCs
53808-1066-1- Official label
- DailyMed (National Library of Medicine), updated Dec 7, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?