NDC 51662-1400
Sodium Bicarbonate 42 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Fresenius Kabi, LLC's NDC 63323-083.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Bicarbonate Ion: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 42 mg per 1 mL
- Approval
- unapproved drug other
- On the market since
- Oct 19, 2019
- Package NDCs
51662-1400-1- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2025
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