NDC 50419-541
Kerendia 20 mg tablet, film coated
On the label: Bayer HealthCare Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| AMPAC Fine Chemicals LLC | Rancho Cordova, CA, United States | Makes the active ingredient | No problems foundSep 10, 2025 · 9 inspections, 1 with FDA action |
| Bayer AG | Leverkusen, Germany | Makes it, tests it, packages it and mills it | Problems found, fixed voluntarilyMar 20, 2025 · 10 inspections, 2 with FDA action |
| Bayer AG | Wuppertal, Germany | Makes the active ingredient and tests it | Problems found, fixed voluntarilyJan 18, 2023 · 8 inspections |
| Bayer AG | Bergkamen, Germany | Tests it | Problems found, fixed voluntarilyNov 14, 2024 · 7 inspections, 1 with FDA action |
| Bayer Aktiengesellschaft | Berlin, Germany | Packages it and mills it | Problems found, fixed voluntarilyJun 16, 2023 · 5 inspections |
| Delpharm Milano SRL | Segrate, Italy | Packages it and labels it | Problems found, fixed voluntarilyFeb 18, 2022 · 5 inspections |
| Sharp Packaging Services, LLC | Allentown, PA, United States | Packages it and labels it | No problems foundNov 21, 2025 · 7 inspections |
Product details
- Generic drug
- Finerenone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- NDA NDA215341
- On the market since
- Jul 9, 2021
- Package NDCs
50419-541-0150419-541-0250419-541-0650419-541-70- Official label
- DailyMed (National Library of Medicine), updated Sep 21, 2026
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