NDC 51662-1542
Etomidate 40 mg per 20 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from AuroMedics Pharma LLC's NDC 55150-222.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Etomidate: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 40 mg per 20 mL
- Approval
- ANDA ANDA206126
- On the market since
- Apr 9, 2022
- Package NDCs
51662-1542-1- Official label
- DailyMed (National Library of Medicine), updated Apr 9, 2022
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