NDC 51662-1547
Vecuronium Bromide 10 mg injection, powder, lyophilized, for 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 55150-235.
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
- Vecuronium: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 10 mg
- Approval
- ANDA ANDA206670
- On the market since
- Jul 31, 2022
- Package NDCs
51662-1547-1- Official label
- DailyMed (National Library of Medicine), updated Feb 22, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?