NDC 63323-851
Hydromorphone Hydrochloride 10 mg per 1 mL injection, solution
On the label: Fresenius Kabi, LLC.
Where it's 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
- Hydromorphone: every company that makes it
- Form
- injection, solution, intramuscular; intravenous; subcutaneous
- Strength
- 10 mg per 1 mL
- Approval
- NDA NDA019034
- On the market since
- Dec 15, 2017
- Package NDCs
63323-851-0363323-851-0763323-851-1063323-851-1563323-851-50- Official label
- DailyMed (National Library of Medicine), updated Jul 15, 2026
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