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NDC 0173-0737, sumatriptan, tablet, film coated, from GlaxoSmithKline LLC.

Product NDC
0173-0737
Status
Listed
Labeler
GlaxoSmithKline LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020132
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0173-0737 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUMATRIPTAN SUCCINATE100 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
0173-0737-01001730737011 CARTON in 1 CARTON (0173-0737-01) / 1 BLISTER PACK in 1 CARTON / 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/584abe73-8290-4484-ff8e-5890831c095e

  • NADAC price for package 00173073701

    GET /v1/drugs/nadac/00173073701

Use it

Look up 0173-0737 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0173-0737 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0173-0737. 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.