Recalls / Brands / Nicardipine Hydrochloride
Nicardipine Hydrochloride
6 FDA drug recalls involving brand “Nicardipine Hydrochloride”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2025-04-18 | Class II | niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, American R | American Regent, Inc. |
| 2025-04-18 | Class II | niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, Mfd for: C | American Regent, Inc. |
| 2024-05-14 | Class II | niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 x 10 mL Single Dose Vials, Rx Only, For | American Regent, Inc. |
| 2024-02-20 | Class II | Nicardipine Hydrochloride Injection (2.5mg/mL), US, 25mg per 10mL, 10mL Vial, Rx only, Distributed by: AuroMe | Eugia US LLC |
| 2024-02-20 | Class II | Nicardipine Hydrochloride Injection, USP 25mg/mL (2.5 mg/mL) 10 mL vials, Distributed by: AuroMedics Pharma LL | Eugia US LLC |
| 2013-05-13 | Class III | Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL), 10 mL single-use vials, Rx Only, Mfd. by Exela Ph | West-ward Pharmaceutical Corp. |