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Sumatriptan

NDC 82804-169, Sumatriptan, tablet, film coated, from Proficient Rx LP.

Product NDC
82804-169
Status
Listed
Labeler
Proficient Rx LP
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/82804-169 \
  -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
82804-169-09828040169091 BLISTER PACK in 1 CARTON (82804-169-09) / 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/85bf8e58-0984-427b-9ed4-7e0df4e444d2

Use it

Look up 82804-169 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-169. 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.