NDC 76045-238
Morphine Sulfate 1 mg per 0.5 mL injection, solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Wilson, NC, United States | Makes it and tests it | Problems found, fixed voluntarilyFeb 13, 2026 · 5 inspections |
Recalls
- Aug 4, 2026 · Class I · Fresenius Kabi USA, LLC
Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
Lots: Lot #: 6402820, Exp. Date 12/2028
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, intramuscular; intravenous
- Strength
- 1 mg per 0.5 mL
- Approval
- NDA NDA204223
- On the market since
- Oct 30, 2013
- Package NDCs
76045-238-0176045-238-10- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2026
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