72064-150 : Ayvakit 50 mg Oral Tablet, Film Coated


NDC: 72064-150
Labeler: Blueprint Medicines Corporation
Product Type: Human Prescription Drug
Drug Name:  Ayvakit
Dosage Form: Oral Tablet, Film Coated
Application #: NDA212608
Rev. Date: 


NDC Package Codes:

  • 72064-150-30: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (72064‑150‑30)

Active Ingredients:

  • Avapritinib

Dosage Strength:

  • 50 mg

Pharmaceutical Classes:

  • Bile Salt Export Pump Inhibitors [MoA]
  • Breast Cancer Resistance Protein Inhibitors [MoA]
  • Cytochrome P450 2C9 Inhibitors [MoA]
  • Kinase Inhibitor [EPC]
  • Multidrug and Toxin Extrusion Transporter 1 Inhibitors [MoA]
  • Multidrug and Toxin Extrusion Transporter 2 K Inhibitors [MoA]
  • P-Glycoprotein Inhibitors [MoA]
  • Tyrosine Kinase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 72064-110 Ayvakit 100 mg Oral Tablet, Film Coated by Blueprint Medicines Corporation
  • 72064-120 Ayvakit 200 mg Oral Tablet, Film Coated by Blueprint Medicines Corporation
  • 72064-125 Ayvakit 25 mg Oral Tablet, Film Coated by Blueprint Medicines Corporation
  • 72064-130 Ayvakit 300 mg Oral Tablet, Film Coated by Blueprint Medicines Corporation

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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.