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Sumatriptan

NDC 70069-804, Sumatriptan, injection, solution, from Somerset Therapeutics, LLC.

Product NDC
70069-804
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213998
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-804 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUMATRIPTAN SUCCINATE6 mg/.5mL

Pharmacologic classes

Serotonin 1b Receptor Agonists [MoA]; Serotonin 1d Receptor Agonists [MoA]; Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Package NDCNDC-11Package
70069-804-01700690804011 VIAL in 1 CARTON (70069-804-01) / .5 mL in 1 VIAL
70069-804-05700690804055 VIAL in 1 CARTON (70069-804-05) / .5 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/53c62307-bd19-4418-b1b0-c0274b5595df

Use it

Look up 70069-804 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-804 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-804. 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.