NDC 51662-1205
Amiodarone Hydrochloride 50 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0143-9875.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Farmaceutica (portugal), S.a | Terrugem Sintra, Portugal | Makes it | Problems found, fixed voluntarilyApr 21, 2023 · 9 inspections, 1 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Amiodarone: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA077234
- On the market since
- Sep 19, 2018
- Package NDCs
51662-1205-151662-1205-251662-1205-3- Official label
- DailyMed (National Library of Medicine), updated Feb 22, 2024
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