Recalls / Generics / Budesonide
Budesonide
5 FDA drug recalls involving generic “Budesonide”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2025-06-30 | Class II | Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manuf | Cipla USA, Inc. |
| 2024-01-08 | Class II | Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, | Teva Pharmaceuticals USA, Inc |
| 2022-09-15 | Class II | Budesonide Inhalation Suspension 0.25mg/2mL, For Inhalation Only, Rx Only, 1 envelope x five 2 mL Single Dose | CIPLA |
| 2013-01-11 | Class III | PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04 | AstraZeneca LP |
| 2013-01-11 | Class III | PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation Suspension NDC: 0186-1989-04 | AstraZeneca LP |