Drugplain

Olumiant 2 mg/1

baricitinib · TABLET, FILM COATED · Eli Lilly and Company

No Recall History
Plain English

Olumiant is a tablet, film coated containing baricitinib at 2 mg/1, taken oral. Manufactured by Eli Lilly and Company.

Key Facts

Brand Name
Olumiant
Generic Name
baricitinib
NDC Code (Product)
0002-4182
Manufacturer
Eli Lilly and Company
Strength
2 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
NDA207924
Drug Class
Janus Kinase Inhibitor [EPC]
Marketing Start
05/31/2018

Recall History

No Recall History

Frequently Asked Questions

What is Olumiant used for?

Olumiant contains baricitinib. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Olumiant a controlled substance?

Olumiant is not classified as a controlled substance by the DEA.

What is the generic name for Olumiant?

The generic name for Olumiant is baricitinib. There are 1 other brand versions of baricitinib.

What is the NDC code for Olumiant 2 mg/1?

The NDC (National Drug Code) for Olumiant 2 mg/1 is 0002-4182, listed by Eli Lilly and Company.

Product NDC

0002-4182

Package NDC

0002-4182-30

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)