Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| B. Braun US Pharmaceutical Manufacturing LLC | Irvine, CA, United States | Makes it, packages it and labels it | Serious problems, FDA actionNov 21, 2025 · 13 inspections, 3 with FDA action |
Recalls
- Apr 2, 2026 · Class II · B Braun Medical Inc
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Lots: Lot # J5H166, J5H167, Exp Date: 30NOV2026.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Anhydrous Dextrose: every company that makes it
- Form
- solution, intravenous
- Strength
- 70 g per 100 mL
- Approval
- NDA NDA019626
- On the market since
- Feb 19, 2015
- Package NDCs
0264-7387-50- Official label
- DailyMed (National Library of Medicine), updated Oct 21, 2026
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