NDC 0404-9882
Ketamine Hydrochloride 50 mg per 1 mL injection, solution, concentrate
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from Hospira, Inc.'s NDC 0409-2053.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Product details
- Generic drug
- Ketamine: every company that makes it
- Form
- injection, solution, concentrate
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA074549
- On the market since
- Jan 11, 2022
- Package NDCs
0404-9882-10- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2024
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