Class II · Moderate risk
niCARdipine Hydrochloride Injection
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
National Drug Code
Is NDC 72572-0470-10 recalled?
Nicardipine Hydrochloride · 10 VIAL in 1 CARTON (72572-470-10) / 10 mL in 1 VIAL (72572-470-01)
Yes — this exact package was recalled
3 FDA recalls name the code 72572-0470-10 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.
2 of these recalls are still ongoing.
- Active ingredient
- nicardipine hydrochloride
- Strength
- NICARDIPINE HYDROCHLORIDE 2.5 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Civica, Inc.
- Type
- Human Prescription Drug
- Product code
- 72572-0470
Recalls naming this package
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.
Class II · Moderate risk
niCARdipine Hydrochloride Injection
Lack of Assurance of Sterility.
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
- 72572-0740 Sodium Bicarbonate 3
- 72572-0021 See recall 1
- 72572-0022 See recall 1
- 72572-0057 See recall 1
- 72572-0058 See recall 1
- 72572-0576 See recall 1
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