NDC 51662-1310
Infant 4.2% 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 Hospira, Inc.'s NDC 0409-5534.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
| Hospira, Inc. | Location not on file | Tests it | Not inspected on record |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Dec 21, 2023 · Class I · Pfizer Inc.
Presence of Particulate Matter; identified as glass
Lots: Lot GX1542, Exp. 01/01/2025 - Oct 2, 2023 · Class I · Pfizer Inc.
Presence of Particulate Matter: identified as glass.
Lots: Lot#: GJ5007, Exp. 8/1/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
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 21, 2018
- Package NDCs
51662-1310-151662-1310-251662-1310-3- Official label
- DailyMed (National Library of Medicine), updated Jun 16, 2025
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