NDC 51662-1710
Rocuronium Bromide 10 mg per 1 mL injection
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0143-9251.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Farmaceutica (portugal), S.a | Terrugem Sintra, Portugal | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 21, 2023 · 9 inspections, 1 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · repackages it
Product details
- Generic drug
- Rocuronium: every company that makes it
- Form
- injection, intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA204679
- On the market since
- Apr 30, 2017
- Package NDCs
51662-1710-1- Official label
- DailyMed (National Library of Medicine), updated Aug 10, 2026
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