NDC 76045-212
Dexamethasone Sodium Phosphate 10 mg per 1 mL injection, emulsion
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Wilson, NC, United States | Makes it and tests it | Problems found, fixed voluntarilyFeb 13, 2026 · 5 inspections |
Product details
- Generic drug
- Dexamethasone: every company that makes it
- Form
- injection, emulsion, intramuscular; intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA209192
- On the market since
- Feb 21, 2024
- Package NDCs
76045-212-0076045-212-10- Official label
- DailyMed (National Library of Medicine), updated Dec 17, 2025
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