NDC 63323-451
Morphine Sulfate 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 |
Recalls
- Sep 17, 2021 · Class II · Fresenius Kabi USA LLC
Defective container: Cracked vials leading to lack of sterility assurance
Lots: Lot # 6023731, 6023732, Exp 03/2023; 6024172, 6024260, Exp 06/2023
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
- 10 mg per 1 mL
- Approval
- NDA NDA204223
- On the market since
- Apr 10, 2018
- Package NDCs
63323-451-0063323-451-01- Official label
- DailyMed (National Library of Medicine), updated Jul 31, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?