NDC 51662-1680
Dextrose 100 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 63323-824.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi Deutschland GmbH | Friedberg, Germany | Makes it, makes the active ingredient and tests it | Problems found, fixed voluntarilyDec 21, 2023 · 4 inspections |
| Fresenius Kabi USA, LLC | Wilson, NC, United States | Makes it and tests it | Problems found, fixed voluntarilyFeb 13, 2026 · 5 inspections |
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
- 100 mg per 1 mL
- Approval
- ANDA ANDA209448
- On the market since
- Mar 29, 2019
- Package NDCs
51662-1680-1- Official label
- DailyMed (National Library of Medicine), updated Mar 16, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?