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Sumatriptan

NDC 63304-097, Sumatriptan, tablet, from SUN PHARMACEUTICAL INDUSTRIES, INC..

Product NDC
63304-097
Status
Listed
Labeler
SUN PHARMACEUTICAL INDUSTRIES, INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076554
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-097 \
  -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
63304-097-1363304009713120 TABLET in 1 BOTTLE (63304-097-13)
63304-097-19633040097191 BLISTER PACK in 1 CARTON (63304-097-19) / 9 TABLET in 1 BLISTER PACK
63304-097-45633040097455 TABLET in 1 BOTTLE (63304-097-45)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c87cf537-9f7f-400e-ac4b-86e6f7e78775

Use it

Look up 63304-097 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-097 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-097. 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.