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MAYZENT

NDC 0078-1014, siponimod, tablet, film coated, from Novartis Pharmaceuticals Corporation.

Product NDC
0078-1014
Status
Listed
Labeler
Novartis Pharmaceuticals Corporation
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA209884
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0078-1014 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SIPONIMOD1 mg/1

Pharmacologic classes

Sphingosine 1-Phosphate Receptor Modulators [MoA]; Sphingosine 1-phosphate Receptor Modulator [EPC]

Package NDCNDC-11Package
0078-1014-150007810141530 TABLET, FILM COATED in 1 BOTTLE (0078-1014-15)
0078-1014-930007810149330 TABLET, FILM COATED in 1 BOTTLE (0078-1014-93)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/44492772-5aed-4627-bd85-e8e89f308bb3

Use it

Look up 0078-1014 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0078-1014 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0078-1014. 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.