Recalls / Active ingredient / Acyclovir Sodium
Acyclovir Sodium
4 FDA drug recalls involving the active ingredient “Acyclovir Sodium” — 2 Class I.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2022-12-28 | Class II | Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx only, Distributed by: Au | Eugia US LLC |
| 2022-09-26 | Class II | Acyclovir Sodium Injection, 500mg/10mL (50mg/mL), 10 mL Single Dose Vial, Rx only, Distributed by: AuroMedics | AuroMedics Pharma LLC |
| 2021-02-18 | Class I | Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01, For Intravenous Infusion Only MUST BE D | Zydus Pharmaceuticals (USA) Inc |
| 2021-02-18 | Class I | Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01, For Intravenous Infusion Only MUST BE | Zydus Pharmaceuticals (USA) Inc |