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PONVORY

NDC 43068-620, Ponesimod, tablet, film coated, from Vanda Pharmaceuticals Inc..

Product NDC
43068-620
Status
Listed
Labeler
Vanda Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA213498
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43068-620 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PONESIMOD20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
43068-620-01430680620011 BOTTLE in 1 CARTON (43068-620-01) / 30 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0c025ba8-ba51-272e-e063-6294a90ad120

Use it

Look up 43068-620 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43068-620 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43068-620. 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.