NDC 51662-1545
Rocuronium Bromide 100 mg per 10 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 55150-226.
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
- 100 mg per 10 mL
- Approval
- ANDA ANDA206206
- On the market since
- Apr 9, 2022
- Package NDCs
51662-1545-1- Official label
- DailyMed (National Library of Medicine), updated Apr 9, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?