Recalls / Active ingredient / Ethosuximide
Ethosuximide
2 FDA drug recalls involving the active ingredient “Ethosuximide”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2021-07-29 | Class II | Ethosuximide Oral Solution USP 250 mg/5 mL, 16 fl oz (473 mL), Rx ONLY, Pharmaceutical Associates, Inc. Green | PAI Holdings, LLC. dba Pharmaceutical Associates Inc |
| 2019-09-12 | Class III | Zarontin (ethosuximide capsules, USP) 250 mg, 100-count bottle, Rx Onl,y Made in Netherlands Distributed by Pa | Pfizer Inc. |