Class I ยท High risk
Morphine Sulfate Injection
Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
National Drug Code
Is NDC 76045-0004-01 recalled?
Morphine Sulfate
Yes — this exact package was recalled
1 FDA recall names the code 76045-0004-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Morphine Sulfate
- Strength
- MORPHINE SULFATE 2 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Fresenius Kabi, USA LLC
- Type
- Human Prescription Drug · DEA CII
- Product code
- 76045-0004
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 76045-0001 Midazolam 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.