NDC 0409-2053
Ketamine Hydrochloride 50 mg per 1 mL injection, solution, concentrate
On the label: Hospira, Inc..
Where it's 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, intramuscular; intravenous
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA074549
- On the market since
- Nov 30, 2004
- Package NDCs
0409-2053-100409-2053-20- Official label
- DailyMed (National Library of Medicine), updated May 12, 2026
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