NDC 70518-0621
Dexamethasone Sodium Phosphate 4 mg per 1 mL injection, solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Fresenius Kabi, LLC's NDC 63323-165.
Where the pills inside were 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
- Strength
- 4 mg per 1 mL
- Approval
- ANDA ANDA084916
- On the market since
- Jul 17, 2017
- Package NDCs
70518-0621-0- Official label
- DailyMed (National Library of Medicine), updated Jul 18, 2017
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