Class II ยท Moderate risk
Infumorph (Preservative-free Morphine Sulfate Sterile Solution)
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
National Drug Code
Is NDC 0641-6039-01 recalled?
Infumorph 200 · 20 mL in 1 AMPULE (0641-6039-01)
Yes — this exact package was recalled
1 FDA recall names the code 0641-6039-01 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 10 mg/mL
- Form
- Injection, Solution · Epidural, Intrathecal
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 0641-6039
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
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