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SCEMBLIX

NDC 0078-1091, asciminib, tablet, film coated, from Novartis Pharmaceuticals Corporation.

Product NDC
0078-1091
Status
Listed
Labeler
Novartis Pharmaceuticals Corporation
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA215358
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0078-1091 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ASCIMINIB HYDROCHLORIDE20 mg/1
Package NDCNDC-11Package
0078-1091-200007810912060 TABLET, FILM COATED in 1 BOTTLE (0078-1091-20)
0078-1091-940007810919414 TABLET, FILM COATED in 1 BOTTLE (0078-1091-94)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e33001e7-3650-42b1-ae56-cddb5c43aa2b

Use it

Look up 0078-1091 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0078-1091 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0078-1091. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.