United States · FDA National Drug Code directory
asciminib
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 17088-0156_ac3ac5d6-dc74-451d-b4b4-f54c5090200f
- Product NDC
- 17088-0156
- Form
- TABLET, FILM COATED
- Composition / generic term
- asciminib
- Labeler
- Novartis Pharma Stein AG
- Marketing category
- DRUG FOR FURTHER PROCESSING
- Marketing start / end (source format)
- 20211029
- Source listing expiry
- 20271231
Source-listed ingredients
- ASCIMINIB HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 25000 TABLET, FILM COATED in 1 DRUM (17088-0156-1) · 17088-0156-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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