NDC 0404-9881
Ketamine Hydrochloride 100 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 0409-2051.
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 |
Repackaging site
- Henry Schein, Inc., Bastian, VA, United States · relabels it
Product details
- Generic drug
- Ketamine: every company that makes it
- Form
- injection, solution, concentrate
- Strength
- 100 mg per 1 mL
- Approval
- ANDA ANDA074549
- On the market since
- Jan 11, 2022
- Package NDCs
0404-9881-05- Official label
- DailyMed (National Library of Medicine), updated May 2, 2024
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