0002-4479 : Olumiant 4 mg Oral Tablet, Film Coated


NDC: 0002-4479
Labeler: Eli Lilly and Company
Product Type: Human Prescription Drug
Drug Name:  Olumiant
Dosage Form: Oral Tablet, Film Coated
Application #: NDA207924
Rev. Date: 


NDC Package Codes:

  • 0002-4479-30: 30 TABLET, FILM COATED IN 1 BOTTLE (0002‑4479‑30)
  • 0002-4479-61: 30 TABLET, FILM COATED IN 1 BOTTLE (0002‑4479‑61)

Active Ingredients:

  • Baricitinib

Dosage Strength:

  • 4 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0002-4182 Olumiant 2 mg Oral Tablet, Film Coated by Eli Lilly and Company
  • 0002-4732 Olumiant 1 mg Oral Tablet, Film Coated by Eli Lilly and Company

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