NDC 63323-165
Dexamethasone Sodium Phosphate 4 mg per 1 mL injection, solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Dexamethasone: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 4 mg per 1 mL
- Approval
- ANDA ANDA084916
- On the market since
- Sep 7, 2000
- Package NDCs
63323-165-0163323-165-0263323-165-0363323-165-0563323-165-1163323-165-1363323-165-3063323-165-5163323-165-53- Official label
- DailyMed (National Library of Medicine), updated Jun 8, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?