NDC 51662-1546
Rocuronium Bromide 50 mg per 5 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 55150-225.
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
Recalls
- Feb 7, 2024 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP Deviations: Products were stored outside the drug label specifications.
Lots: 1064081
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Rocuronium: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 50 mg per 5 mL
- Approval
- ANDA ANDA206206
- On the market since
- Jul 18, 2021
- Package NDCs
51662-1546-1- Official label
- DailyMed (National Library of Medicine), updated Feb 19, 2024
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