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Zolmitriptan

NDC 71626-101, Zolmitriptan, tablet, film coated, from Medstone Pharma LLC.

Product NDC
71626-101
Status
Listed
Labeler
Medstone Pharma LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207867
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71626-101 \
  -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
71626-101-06716260101066 BLISTER PACK in 1 CARTON (71626-101-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c970dd17-abdb-4fac-8de8-984e388b498c

  • NADAC price for package 71626010106

    GET /v1/drugs/nadac/71626010106

Use it

Look up 71626-101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71626-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71626-101. 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.