Recalls / Active ingredient / Lovastatin
Lovastatin
2 FDA drug recalls involving the active ingredient “Lovastatin”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2019-02-19 | Class III | Lovastatin Tablets USP, 40 mg, packaged in a) 100-count bottles (NDC 68001-316-00) and b)1000-count bottles (N | American Health Packaging |
| 2019-02-13 | Class III | Lovastatin Tablets USP, 40 mg, packaged in a) 60-count (NDC 68180-469-07 and b) 100-count (NDC 68180-469-01) b | Lupin Pharmaceuticals Inc. |