Package 0002-6885-30

Brand: baricitinib

Generic: baricitinib
NDC Package

Package Facts

Identity

Package NDC 0002-6885-30
Digits Only 0002688530
Product NDC 0002-6885
Product ID 0002-6885_14a2ffe3-1d7e-4d1b-ac44-1698d5f92da4
Description

30 TABLET, FILM COATED in 1 BOTTLE (0002-6885-30)

Marketing

Marketing Status
Marketed Since 2021-12-20
Brand baricitinib
Generic baricitinib
Sample Package No

Linked Drug Pages (1)

Baricitinib ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "14a2ffe3-1d7e-4d1b-ac44-1698d5f92da4", "openfda": {"nui": ["N0000190858", "N0000190857"], "unii": ["ISP4442I3Y"], "rxcui": ["2588561"], "spl_set_id": ["7052c055-fedf-453b-86bc-01f5465eb157"], "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 (0002-6885-30)", "package_ndc": "0002-6885-30", "marketing_start_date": "20211220"}], "brand_name": "Baricitinib", "product_id": "0002-6885_14a2ffe3-1d7e-4d1b-ac44-1698d5f92da4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Janus Kinase Inhibitor [EPC]", "Janus Kinase Inhibitors [MoA]"], "product_ndc": "0002-6885", "generic_name": "baricitinib", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baricitinib", "active_ingredients": [{"name": "BARICITINIB", "strength": "4 mg/1"}], "marketing_category": "EMERGENCY USE AUTHORIZATION", "marketing_start_date": "20211220", "listing_expiration_date": "20261231"}