NDC 0409-4264
Hydromorphone Hydrochloride 0.5 mg per 0.5 mL injection, solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
| 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
- Hydromorphone: every company that makes it
- Form
- injection, solution, intramuscular; intravenous; subcutaneous
- Strength
- 0.5 mg per 0.5 mL
- Approval
- NDA NDA200403
- On the market since
- May 27, 2022
- Package NDCs
0409-4264-010409-4264-11- Official label
- DailyMed (National Library of Medicine), updated Feb 4, 2026
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