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ELEPSIA XR 1000 MG

NDC 80705-100, levetiracetam, tablet, extended release, from TRIPOINT THERAPEUTICS, LLC.

Product NDC
80705-100
Status
Listed
Labeler
TRIPOINT THERAPEUTICS, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA204417
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80705-100 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVETIRACETAM1000 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
80705-100-02807050100021 BLISTER PACK in 1 CARTON (80705-100-02) / 2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
80705-100-308070501003030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80705-100-30)
80705-100-99807050100991 BLISTER PACK in 1 CARTON (80705-100-99) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cac83d47-88a2-4447-a0c0-90b44ffda0ac

Use it

Look up 80705-100 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80705-100 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80705-100. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.