Recalls / Active ingredient / Levodopa
Levodopa
3 FDA drug recalls involving the active ingredient “Levodopa”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2025-10-07 | Class II | Carbidopa, Levodopa, Entacapone Tablets, 25 mg/100 mg/200 mg, 100-count bottle, Rx Only, Manufactured for: Ris | Rising Pharma Holding, Inc. |
| 2017-01-13 | Class II | Duopa (carbidopa and levodopa enteral suspension), 4.63 mg/20 mg per mL, 100 mL cassette, 7 cassettes per cart | AbbVie Inc. |
| 2017-01-12 | Class II | Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg a) 100-count bottles (NDC 62756-519-88), b) 500-cou | Sun Pharmaceutical Industries, Inc. |