0003-0895 : Sotyktu 6 mg Oral Tablet, Film Coated


NDC: 0003-0895
Labeler: E.r. Squibb & Sons, L.L.C.
Product Type: Human Prescription Drug
Drug Name:  Sotyktu
Dosage Form: Oral Tablet, Film Coated
Application #: NDA214958
Rev. Date: 


NDC Package Codes:

  • 0003-0895-11: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (0003‑0895‑11)
  • 0003-0895-91: 30 TABLET, FILM COATED IN 1 BLISTER PACK (0003‑0895‑91)

Active Ingredients:

  • Deucravacitinib

Dosage Strength:

  • 6 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.