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Sumatriptan

NDC 68071-3525, Sumatriptan, tablet, film coated, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-3525
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
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/68071-3525 \
  -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
68071-3525-9680713525091 BLISTER PACK in 1 CARTON (68071-3525-9) / 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/082d05f6-3850-0fa2-e063-6294a90a0c66

Use it

Look up 68071-3525 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3525 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3525. 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.