0002-1717 : Inluriyo 200 mg Oral Tablet, Film Coated


NDC: 0002-1717
Labeler: Eli Lilly and Company
Product Type: Human Prescription Drug
Drug Name:  Inluriyo
Dosage Form: Oral Tablet, Film Coated
Application #: NDA218881
Rev. Date: 


NDC Package Codes:

  • 0002-1717-28: 28 TABLET, FILM COATED IN 1 BOTTLE (0002‑1717‑28)
  • 0002-1717-56: 56 TABLET, FILM COATED IN 1 BOTTLE (0002‑1717‑56)

Active Ingredients:

  • Imlunestrant

Dosage Strength:

  • 200 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.