Class III · Low risk
Nicardipine Hydrochloride Injection 25 mg/10 mL
Failed Impurity/Degradation Specifications; out of specification value for impurity Nitrophenylpuridine Derivative (NPP-D)
National Drug Code
Is NDC 0143-9689-10 recalled?
Nicardipine Hydrochloride · 10 VIAL in 1 CARTON (0143-9689-10) / 10 mL in 1 VIAL (0143-9689-01)
Yes — this exact package was recalled
1 FDA recall names the code 0143-9689-10 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.
- Active ingredient
- Nicardipine Hydrochloride
- Strength
- NICARDIPINE HYDROCHLORIDE 25 mg/10mL
- Form
- Injection · Intravenous
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 0143-9689
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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