Package 0003-0895-91

Brand: sotyktu

Generic: deucravacitinib
NDC Package Sample

Package Facts

Identity

Package NDC 0003-0895-91
Digits Only 0003089591
Product NDC 0003-0895
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0003-0895-91)

Marketing

Marketing Status
Marketed Since 2022-09-09
Brand sotyktu
Generic deucravacitinib
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff4d7258-5068-4cdf-9692-8cae04c3198e", "openfda": {"nui": ["N0000194043", "N0000194044"], "unii": ["N0A21N6RAU"], "rxcui": ["2612092", "2612098"], "spl_set_id": ["ff4d7258-5068-4cdf-9692-8cae04c3198e"], "pharm_class_epc": ["Tyrosine Kinase 2 Inhibitor [EPC]"], "pharm_class_moa": ["Tyrosine Kinase 2 Inhibitors [MoA]"], "manufacturer_name": ["E.R. Squibb & Sons, L.L.C."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0003-0895-11)", "package_ndc": "0003-0895-11", "marketing_start_date": "20220909"}, {"sample": true, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0003-0895-91)", "package_ndc": "0003-0895-91", "marketing_start_date": "20220909"}], "brand_name": "SOTYKTU", "product_id": "0003-0895_ff4d7258-5068-4cdf-9692-8cae04c3198e", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0003-0895", "generic_name": "deucravacitinib", "labeler_name": "E.R. Squibb & Sons, L.L.C.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOTYKTU", "active_ingredients": [{"name": "DEUCRAVACITINIB", "strength": "6 mg/1"}], "application_number": "NDA214958", "marketing_category": "NDA", "marketing_start_date": "20220909", "listing_expiration_date": "20261231"}