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Sumatriptan

NDC 71921-170, sumatriptan, spray, from Florida Pharmaceutical Products, LLC..

Product NDC
71921-170
Status
Listed
Labeler
Florida Pharmaceutical Products, LLC.
Dosage form
SPRAY
Route
NASAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208967
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71921-170 \
  -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
71921-170-61719210170616 CONTAINER in 1 BOX (71921-170-61) / 1 SPRAY in 1 CONTAINER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/267dadc1-6960-4d8b-88ef-86be9c5f7159

Use it

Look up 71921-170 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71921-170 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71921-170. 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.