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Sumatriptan Succinate

NDC 72189-432, Sumatriptan Succinate, tablet, film coated, from Direct_Rx.

Product NDC
72189-432
Status
Listed
Labeler
Direct_Rx
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078295
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-432 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUMATRIPTAN SUCCINATE25 mg/1

Pharmacologic classes

Serotonin 1b Receptor Agonists [MoA]; Serotonin 1d Receptor Agonists [MoA]; Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Package NDCNDC-11Package
72189-432-09721890432099 TABLET, FILM COATED in 1 BOTTLE (72189-432-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f6c95873-576d-a1c2-e053-6294a90a3ff9

Use it

Look up 72189-432 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-432 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-432. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.