Class II · Moderate risk
Nicardipine Hydrochloride Injection
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
National Drug Code
Is NDC 55150-0183-11 recalled?
Nicardipine Hydrochloride · 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-183-11) / 10 mL in 1 VIAL, SINGLE-DOSE (55150-183-02)
Yes — this exact package was recalled
1 FDA recall names the code 55150-0183-11 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 25 mg/10mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Eugia US LLC
- Type
- Human Prescription Drug
- Product code
- 55150-0183
Recalls naming this package
Class II · Moderate risk
Nicardipine Hydrochloride Injection
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
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
- 55150-0120 Piperacillin and Tazobactam 2
- 55150-0202 Pantoprazole Sodium 2
- 55150-0242 Linezolid 2
- 55150-0243 Levofloxacin 2
- 55150-0306 Progesterone 2
- 55150-0113 Ampicillin 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.