Class II ยท Moderate risk
CLEVIPREX (clevidipine injectable emulsion)
Lack of Assurance of Sterility
National Drug Code
Is NDC 10122-0611-10 recalled?
Cleviprex · 10 CARTON in 1 CARTON (10122-611-10) / 1 VIAL, SINGLE-USE in 1 CARTON (10122-611-01) / 100 mL in 1 VIAL, SINGLE-USE
Yes — this exact package was recalled
1 FDA recall names the code 10122-0611-10 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
- clevipidine
- Strength
- CLEVIDIPINE .5 mg/mL
- Form
- Emulsion · Intravenous
- Labeler
- Chiesi USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 10122-0611
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
- 10122-0502 Revcovi 1
- 10122-0510 Curosurf 1
- 10122-0820 Bethkis 1
- 10122-0902 See recall 1
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