NDC 0641-6151
Hydromorphone Hydrochloride 2 mg per 1 mL injection
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Pharmaceuticals USA Inc. | Cherry Hill, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundMay 13, 2026 · 18 inspections |
Product details
- Generic drug
- Hydromorphone: every company that makes it
- Form
- injection, intramuscular; intravenous; subcutaneous
- Strength
- 2 mg per 1 mL
- Approval
- ANDA ANDA202159
- On the market since
- Jul 1, 2018
- Package NDCs
0641-6151-010641-6151-25- Official label
- DailyMed (National Library of Medicine), updated Jul 30, 2026
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