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Zolmitriptan

NDC 65862-915, Zolmitriptan, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-915
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207021
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-915 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZOLMITRIPTAN5 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
65862-915-64658620915641 BLISTER PACK in 1 CARTON (65862-915-64) / 3 TABLET, FILM COATED in 1 BLISTER PACK (65862-915-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9212b076-b1ae-4c06-bd56-0ae3c5c9acdf

Use it

Look up 65862-915 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-915 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-915. 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.