NDC 51662-1584
Dextrose monohydrate 25 g per 50 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from International Medication Systems, Ltd.'s NDC 76329-3302.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| International Medication Systems, Ltd. | South El Monte, CA, United States | Makes it and tests it | Serious problems, FDA actionDec 19, 2025 · 15 inspections, 1 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Anhydrous Dextrose: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 25 g per 50 mL
- Approval
- ANDA ANDA203451
- On the market since
- Feb 11, 2022
- Package NDCs
51662-1584-151662-1584-251662-1584-3- Official label
- DailyMed (National Library of Medicine), updated Feb 22, 2024
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