NDC 0143-9391
Remifentanil Hydrochloride 1 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
| Navinta LLC | Ewing, NJ, United States | Tests it | No problems foundSep 30, 2024 · 6 inspections, 1 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 ANDA210594
- On the market since
- May 15, 2021
- Package NDCs
0143-9391-010143-9391-10- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2024
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