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Lunesta

NDC 80725-012, ESZOPICLONE, tablet, coated, from Waylis Therapeutics LLC.

Product NDC
80725-012
Status
Listed
Labeler
Waylis Therapeutics LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021476
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80725-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ESZOPICLONE3 mg/1
Package NDCNDC-11Package
80725-012-308072500123030 TABLET, COATED in 1 BOTTLE (80725-012-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3821f4b7-a3c8-4920-ba80-18aa96532c09

Use it

Look up 80725-012 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80725-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80725-012. 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.