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Sumatriptan

NDC 80425-0475, Sumatriptan, tablet, film coated, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0475
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078284
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0475 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUMATRIPTAN SUCCINATE50 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
80425-0475-1804250475011 BLISTER PACK in 1 CARTON (80425-0475-1) / 9 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2aab8786-b225-833a-e063-6394a90ac7ae

Use it

Look up 80425-0475 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0475 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0475. 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.