NDC 0641-6039
Infumorph 200 10 mg per 1 mL injection, solution
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 and labels it | No problems foundMay 13, 2026 · 18 inspections |
Recalls
- Mar 12, 2024 · Class II · Hikma Pharmaceuticals USA Inc.
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
Lots: Lot #: 052001, 052003, Exp. Date 11/2024; 023012, 023014, Exp. Date 08/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Morphine: every company that makes it
- Form
- injection, solution, epidural; intrathecal
- Strength
- 10 mg per 1 mL
- Approval
- NDA NDA018565
- On the market since
- Sep 18, 1984
- Package NDCs
0641-6039-01- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2025
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