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Zolmitriptan

NDC 69097-863, Zolmitriptan, tablet, film coated, from Cipla USA Inc..

Product NDC
69097-863
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204284
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-863 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZOLMITRIPTAN2.5 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
69097-863-17690970863171 BLISTER PACK in 1 CARTON (69097-863-17) / 6 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/16e520fe-2f57-400b-8ee5-9a3f89037d6c

Use it

Look up 69097-863 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-863 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-863. 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.