Recalls / Active ingredient / Aminophylline Dihydrate
Aminophylline Dihydrate
1 FDA drug recall involving the active ingredient “Aminophylline Dihydrate”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2022-09-27 | Class II | Aminophylline Injection, USP 250 mg/10 mL (25 mg/mL) 25x10 mL Single-dose vial, Rx only, Distributed by Hospi | Pfizer Inc. |