Olumiant

Active Ingredient(s): Baricitinib
FDA Approved: * May 31, 2018
Pharm Company: * ELI LILLY AND CO
Category: Arthritis

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Olumiant Overview

Baricitinib, sold under the brand name Olumiant among others, is a drug for the treatment of rheumatoid arthritis (RA) in adults whose disease was not well controlled by tumor necrosis factor (TNF) inhibitors.[6] It acts as an inhibitor of janus kinase (JAK), blocking the subtypes JAK1 and JAK2.[7] The drug is approved for medical use in the European Union[5] and in the United States.[6][8]An important side effect...

Read more Olumiant Details
Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Baricitinib

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NDC Database Records for Olumiant: (2 results)

Sorted by National Drug Code

• 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

Other drugs which contain Baricitinib or a similar ingredient: (1 result)

• BARICITINIB