NDC 63323-725
Remifentanil Hydrochloride 1 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
Product details
- Generic drug
- Remifentanil: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA206223
- On the market since
- Jan 19, 2018
- Package NDCs
63323-725-0163323-725-10- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2024
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