NDC 0002-4182 – Olumiant

Baricitinib 2 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0002-4182

Product details

Brand name
Olumiant
Generic name
Baricitinib
Labeler
Eli Lilly and Company
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA207924
Marketed since
May 31, 2018
Listing expires
December 31, 2027
Pharmacologic class
Janus Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Olumiant →

Package NDC codes (2)

Package NDCDescriptionSince
0002-4182-3030 TABLET, FILM COATED in 1 BOTTLE (0002-4182-30)May 31, 2018
0002-4182-61 sample30 TABLET, FILM COATED in 1 BOTTLE (0002-4182-61)May 31, 2018

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