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Eletriptan Hydrobromide

NDC 0093-8310, Eletriptan Hydrobromide, tablet, film coated, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-8310
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202040
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-8310 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ELETRIPTAN HYDROBROMIDE20 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
0093-8310-18000938310186 BLISTER PACK in 1 CARTON (0093-8310-18) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-8310-19)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/62dc12ce-4f19-41c6-9593-3cae29f04af1

  • NADAC price for package 00093831018

    GET /v1/drugs/nadac/00093831018

Use it

Look up 0093-8310 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-8310 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-8310. 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.