NDC 50419-542 – Kerendia

Finerenone 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50419-542

Product details

Brand name
Kerendia
Generic name
finerenone
Labeler
Bayer HealthCare Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA215341
Marketed since
July 9, 2021
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Mineralocorticoid-Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Kerendia →

Package NDC codes (4)

Package NDCDescriptionSince
50419-542-0130 TABLET in 1 BOTTLE, PLASTIC (50419-542-01)Jul 11, 2025
50419-542-0290 TABLET in 1 BOTTLE, PLASTIC (50419-542-02)Jul 11, 2025
50419-542-0610 TABLET in 1 BLISTER PACK (50419-542-06)Jul 11, 2025
50419-542-707 TABLET in 1 BOTTLE, PLASTIC (50419-542-70)Jul 11, 2025

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