Class II · Moderate risk
niCARdipine Hydrochloride Injection
Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
National Drug Code
Is NDC 0517-0735-10 recalled?
Nicardipine Hydrochloride · 10 VIAL in 1 CARTON (0517-0735-10) / 10 mL in 1 VIAL (0517-0735-01)
Yes — this exact package was recalled
1 FDA recall names the code 0517-0735-10 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
- nicardipine hydrochloride
- Strength
- NICARDIPINE HYDROCHLORIDE 2.5 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- American Regent, Inc.
- Type
- Human Prescription Drug
- Product code
- 0517-0735
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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