65597-511 : Vanflyta 26.5 mg Oral Tablet, Film Coated


NDC: 65597-511
Labeler: Daiichi Sankyo Inc.
Product Type: Human Prescription Drug
Drug Name:  Vanflyta
Dosage Form: Oral Tablet, Film Coated
Application #: NDA216993
Rev. Date: 


NDC Package Codes:

  • 65597-511-04: 1 BOTTLE IN 1 CARTON (65597‑511‑04) / 14 TABLET, FILM COATED IN 1 BOTTLE
  • 65597-511-28: 1 BOTTLE IN 1 CARTON (65597‑511‑28) / 28 TABLET, FILM COATED IN 1 BOTTLE

Active Ingredients:

  • Quizartinib Dihydrochloride

Dosage Strength:

  • 26.5 mg

Related Products:

Based on records with the same trade name.
  • 65597-504 Vanflyta 17.7 mg Oral Tablet, Film Coated by Daiichi Sankyo 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.