73150-200 : Ukoniq 260.2 mg Oral Tablet, Film Coated


NDC: 73150-200
Labeler: Tg Therapeutics, Inc.
Product Type: Human Prescription Drug
Drug Name:  Ukoniq
Dosage Form: Oral Tablet, Film Coated
Application #: NDA213176
Rev. Date: 


NDC Package Codes:

  • 73150-200-12: 4 CARTON IN 1 CASE (73150‑200‑12) > 12 BOTTLE, PLASTIC IN 1 CARTON > 120 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Umbralisib Tosylate

Dosage Strength:

  • 260.2 mg

Pharmaceutical Classes:

  • Kinase Inhibitor [EPC]
  • Kinase Inhibitors [MoA]

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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.