50419-541 : Kerendia 20 mg Oral Tablet, Film Coated


NDC: 50419-541
Labeler: Bayer Healthcare Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Kerendia
Dosage Form: Oral Tablet, Film Coated
Application #: NDA215341
Rev. Date: 


NDC Package Codes:

  • 50419-541-01: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (50419‑541‑01)
  • 50419-541-02: 90 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (50419‑541‑02)
  • 50419-541-70: 7 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (50419‑541‑70)

Active Ingredients:

  • Finerenone

Dosage Strength:

  • 20 mg

Pharmaceutical Classes:

  • Mineralocorticoid Receptor Antagonists [MoA]
  • Nonsteroidal Mineralocorticoid-Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 50419-540 Kerendia 10 mg Oral Tablet, Film Coated by Bayer Healthcare Pharmaceuticals Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.