Recalls / Active ingredient / Acyclovir
Acyclovir
5 FDA drug recalls involving the active ingredient “Acyclovir”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2021-04-21 | Class III | Acyclovir Tablets, USP, 400 mg, 100 Tablets, Rx Only, Distributed by: Avet Pharmaceuticals Inc., East Brunswic | Heritage Pharmaceuticals Inc |
| 2019-04-25 | Class II | Acyclovir Tablets, USP, 400 mg, 100 count bottles, Rx Only Manufactured by: Cadila Healthcare Ltd., India Dist | Zydus Pharmaceuticals USA Inc |
| 2018-02-09 | Class II | Acyclovir Tablets, USP, 400 mg, 50 Tablets (5 x 10) unit dose blisters [NDC 50268-061-11] per carton [NDC 5026 | Apace KY LLC |
| 2017-04-27 | Class III | Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Pis | Hetero USA Inc |
| 2013-07-17 | Class II | Acyclovir Tablets USP 800 mg ,(NDC 60505-5307-1), Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Can | Apotex Inc. |