olumiant

Generic: baricitinib

Labeler: eli lilly and company
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name olumiant
Generic Name baricitinib
Labeler eli lilly and company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

baricitinib 1 mg/1

Manufacturer
Eli Lilly and Company

Identifiers & Regulatory

Product NDC 0002-4732
Product ID 0002-4732_bbb6b499-c2c4-4ef1-a71e-e7a92f0bdbc1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA207924
Listing Expiration 2027-12-31
Marketing Start 2019-10-08

Pharmacologic Class

Established (EPC)
janus kinase inhibitor [epc]
Mechanism of Action
janus kinase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00024732
Hyphenated Format 0002-4732

Supplemental Identifiers

RxCUI
2047241 2047247 2205472 2205474 2588561 2601725
UNII
ISP4442I3Y
NUI
N0000190858 N0000190857

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name olumiant (source: ndc)
Generic Name baricitinib (source: ndc)
Application Number NDA207924 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (0002-4732-30)
source: ndc

Packages (1)

0002-4732-30 30 TABLET, FILM COATED in 1 BOTTLE (0002-4732-30)

Ingredients (1)

baricitinib (1 mg/1)

Linked Drug Pages (1)

Olumiant ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bbb6b499-c2c4-4ef1-a71e-e7a92f0bdbc1", "openfda": {"nui": ["N0000190858", "N0000190857"], "unii": ["ISP4442I3Y"], "rxcui": ["2047241", "2047247", "2205472", "2205474", "2588561", "2601725"], "spl_set_id": ["866e9f35-9035-4581-a4b1-75a621ab55cf"], "pharm_class_epc": ["Janus Kinase Inhibitor [EPC]"], "pharm_class_moa": ["Janus Kinase Inhibitors [MoA]"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0002-4732-30)", "package_ndc": "0002-4732-30", "marketing_start_date": "20191008"}], "brand_name": "Olumiant", "product_id": "0002-4732_bbb6b499-c2c4-4ef1-a71e-e7a92f0bdbc1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Janus Kinase Inhibitor [EPC]", "Janus Kinase Inhibitors [MoA]"], "product_ndc": "0002-4732", "generic_name": "baricitinib", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olumiant", "active_ingredients": [{"name": "BARICITINIB", "strength": "1 mg/1"}], "application_number": "NDA207924", "marketing_category": "NDA", "marketing_start_date": "20191008", "listing_expiration_date": "20271231"}