Package 0078-1091-20
Brand: scemblix
Generic: asciminibPackage Facts
Identity
Package NDC
0078-1091-20
Digits Only
0078109120
Product NDC
0078-1091
Description
60 TABLET, FILM COATED in 1 BOTTLE (0078-1091-20)
Marketing
Marketing Status
Brand
scemblix
Generic
asciminib
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e187165a-eb84-4ee5-98b8-d4e777ec7b4a", "openfda": {"upc": ["0300781098204", "0300781091205"], "unii": ["C5U34S9XFV"], "rxcui": ["2584320", "2584326", "2584328", "2584330", "2680278", "2680280"], "spl_set_id": ["e33001e7-3650-42b1-ae56-cddb5c43aa2b"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (0078-1091-20)", "package_ndc": "0078-1091-20", "marketing_start_date": "20211029"}, {"sample": true, "description": "14 TABLET, FILM COATED in 1 BOTTLE (0078-1091-94)", "package_ndc": "0078-1091-94", "marketing_start_date": "20211029"}], "brand_name": "SCEMBLIX", "product_id": "0078-1091_e187165a-eb84-4ee5-98b8-d4e777ec7b4a", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0078-1091", "generic_name": "asciminib", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SCEMBLIX", "active_ingredients": [{"name": "ASCIMINIB HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "NDA215358", "marketing_category": "NDA", "marketing_start_date": "20211029", "listing_expiration_date": "20261231"}