64842-0120 : Lytgobi 4 mg Oral Tablet


NDC: 64842-0120
Labeler: Taiho Pharmaceutical Co., Ltd.
Product Type: Human Prescription Drug
Drug Name:  Lytgobi
Dosage Form: Oral Tablet
Application #: NDA214801
Rev. Date: 


NDC Package Codes:

  • 64842-0120-4: 1 BLISTER PACK IN 1 CARTON (64842‑0120‑4) / 21 TABLET IN 1 BLISTER PACK
  • 64842-0120-5: 1 BLISTER PACK IN 1 CARTON (64842‑0120‑5) / 28 TABLET IN 1 BLISTER PACK
  • 64842-0120-6: 1 BLISTER PACK IN 1 CARTON (64842‑0120‑6) / 35 TABLET IN 1 BLISTER PACK

Active Ingredients:

  • Futibatinib

Dosage Strength:

  • 4 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.