NDC 0404-9759
Ketamine Hydrochloride 100 mg per 1 mL injection
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from Fresenius Kabi USA, LLC's NDC 65219-186.
Where the pills inside were 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
- 100 mg per 1 mL
- Approval
- ANDA ANDA215808
- On the market since
- Sep 8, 2026
- Package NDCs
0404-9759-05- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2026
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