58468-0251 : Wayrilz 400 mg Oral Tablet, Film Coated


NDC: 58468-0251
Labeler: Genzyme Corporation
Product Type: Human Prescription Drug
Drug Name:  Wayrilz
Dosage Form: Oral Tablet, Film Coated
Application #: NDA219685
Rev. Date: 


NDC Package Codes:

  • 58468-0251-5: 2 BLISTER PACK IN 1 CARTON (58468‑0251‑5) / 28 TABLET, FILM COATED IN 1 BLISTER PACK (58468‑0251‑0)
  • 58468-0251-6: 1 BOTTLE IN 1 CARTON (58468‑0251‑6) / 60 TABLET, FILM COATED IN 1 BOTTLE

Active Ingredients:

  • Rilzabrutinib

Dosage Strength:

  • 400 mg

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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.