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ESZOPICLONE

NDC 65862-969, ESZOPICLONE, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-969
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208451
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-969 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ESZOPICLONE3 mg/1
Package NDCNDC-11Package
65862-969-0165862096901100 TABLET, FILM COATED in 1 BOTTLE (65862-969-01)
65862-969-306586209693030 TABLET, FILM COATED in 1 BOTTLE (65862-969-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f18cc76f-82aa-4ad7-b8ce-5737733ee104

  • NADAC price for package 65862096901

    GET /v1/drugs/nadac/65862096901

Use it

Look up 65862-969 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-969 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-969. 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.