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Sumatriptan

NDC 69097-644, Sumatriptan, spray, from Cipla USA Inc..

Product NDC
69097-644
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
SPRAY
Route
NASAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214209
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-644 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUMATRIPTAN20 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
69097-644-48690970644486 CONTAINER in 1 BOX (69097-644-48) / 1 SPRAY in 1 CONTAINER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/559cca31-c0d2-45bf-999d-e92fc49a4a89
  • NADAC price for package 69097064448

    GET /v1/drugs/nadac/69097064448

Use it

Look up 69097-644 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-644 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-644. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.