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 |
Recalls
- Aug 28, 2012 · Class II · Hospira Inc.
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial
Lots: Lot 15-065-DK, Exp 1SEP2013
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; intravenous
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA073510
- On the market since
- Jun 29, 2005
- Package NDCs
0409-3815-110409-3815-12- Official label
- DailyMed (National Library of Medicine), updated Apr 21, 2026
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