Baricitinib
Tablet, Film Coated · Oral
No FDA structured label text is available for Baricitinib. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Baricitinib in 1 product
Baricitinib NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 0002-6885 | Baricitinib 4 mg/1 Tablet, Film Coated | Eli Lilly and Company | EMERGENCY USE AUTHORIZATION |
Frequently asked questions
Who makes Baricitinib?
Baricitinib is listed by 1 labeler in the FDA NDC directory, including Eli Lilly and Company.