NDC 65219-188
ketamine hydrochloride 50 mg per 1 mL injection
On the label: Fresenius Kabi USA, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
Product details
- Generic drug
- Ketamine: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA215808
- On the market since
- Jul 10, 2023
- Package NDCs
65219-188-0165219-188-10- Official label
- DailyMed (National Library of Medicine), updated Apr 23, 2025
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