New drug applications approved by US FDA as of 01-15 July 2021 which includes New Molecular Entities (NMEs) and new biologics. It does not include Tentative Approvals. Supplemental approvals may have occurred since the original approval date.
KERENDIA
- Active Ingredient(s): Finerenone
- Strength: 10MG; 20MG
- Dosage Form(s) / Route(s): Tablet; Oral
- Company: Bayer Healthcare Pharms
- Approval Date: 09 July 2021
- Submission Classification: Type 1 - New Molecular Entity
- Indication(s): Indicated to reduce the risk of sustained eGFR decline, end stage kidney
disease, cardiovascular death, non-fatal myocardial infarction, and
hospitalization for heart failure in adult patients with chronic kidney disease
(CKD) associated with type 2 diabetes (T2D)
- Approved Label: 09 July 2021 (PDF)