NDC 51662-1609
0.9% Sodium Chloride 9 g per 1000 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Laboratorios Grifols Sa's NDC 76297-001.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Laboratorios Grifols, S. A. | Las Torres de Cotillas, Spain | Makes it, packages it and labels it | Problems found, fixed voluntarilySep 10, 2025 · 4 inspections |
| Laboratorios Grifols, S.A. | Parets del Valles, Spain | Makes it, packages it and labels it | Problems found, fixed voluntarilyOct 27, 2023 · 5 inspections |
| Laboratorios Grifols, S.A. | Parets del Valles, Spain | Tests it | Problems found, fixed voluntarilyOct 27, 2023 · 5 inspections |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Chloride Ion: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 9 g per 1000 mL
- Approval
- ANDA ANDA207956
- On the market since
- Jul 31, 2022
- Package NDCs
51662-1609-1- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2024
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