NDC 50419-540

Kerendia 10 mg tablet, film coated

On the label: Bayer HealthCare Pharmaceuticals Inc..

Germany: 2United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
AMPAC Fine Chemicals LLCRancho Cordova, CA, United StatesMakes the active ingredient No problems foundSep 10, 2025 · 9 inspections, 1 with FDA action
Bayer AGLeverkusen, GermanyMakes it, tests it, packages it and mills it Problems found, fixed voluntarilyMar 20, 2025 · 10 inspections, 2 with FDA action
Bayer AGWuppertal, GermanyMakes the active ingredient and tests it Problems found, fixed voluntarilyJan 18, 2023 · 8 inspections
Bayer AGBergkamen, GermanyTests it Problems found, fixed voluntarilyNov 14, 2024 · 7 inspections, 1 with FDA action
Bayer AktiengesellschaftBerlin, GermanyPackages it and mills it Problems found, fixed voluntarilyJun 16, 2023 · 5 inspections
Delpharm Milano SRLSegrate, ItalyPackages it and labels it Problems found, fixed voluntarilyFeb 18, 2022 · 5 inspections
Sharp Packaging Services, LLCAllentown, PA, United StatesPackages 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
10 mg
Approval
NDA NDA215341
On the market since
Jul 9, 2021
Package NDCs
50419-540-01 50419-540-02 50419-540-06 50419-540-70
Official label
DailyMed (National Library of Medicine), updated Sep 21, 2026

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