NDC 0143-9875
Amiodarone Hydrochloride 50 mg per 1 mL injection, solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's 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 |
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
- Feb 25, 2008
- Package NDCs
0143-9875-010143-9875-100143-9875-25- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2024
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