scemblix
Generic: asciminib
Labeler: novartis pharmaceuticals corporationDrug Facts
Product Profile
Brand Name
scemblix
Generic Name
asciminib
Labeler
novartis pharmaceuticals corporation
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
asciminib hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0078-1196
Product ID
0078-1196_e187165a-eb84-4ee5-98b8-d4e777ec7b4a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA215358
Listing Expiration
2026-12-31
Marketing Start
2021-10-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00781196
Hyphenated Format
0078-1196
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
scemblix (source: ndc)
Generic Name
asciminib (source: ndc)
Application Number
NDA215358 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE (0078-1196-20)
Packages (1)
Ingredients (1)
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 (0078-1196-20)", "package_ndc": "0078-1196-20", "marketing_start_date": "20240418"}], "brand_name": "SCEMBLIX", "product_id": "0078-1196_e187165a-eb84-4ee5-98b8-d4e777ec7b4a", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0078-1196", "generic_name": "asciminib", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SCEMBLIX", "active_ingredients": [{"name": "ASCIMINIB HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "NDA215358", "marketing_category": "NDA", "marketing_start_date": "20211029", "listing_expiration_date": "20261231"}