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ESZOPICLONE

NDC 47335-588, ESZOPICLONE, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-588
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091103
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-588 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ESZOPICLONE3 mg/1
Package NDCNDC-11Package
47335-588-0847335058808100 TABLET, FILM COATED in 1 BOTTLE (47335-588-08)
47335-588-18473350588181000 TABLET, FILM COATED in 1 BOTTLE (47335-588-18)
47335-588-834733505888330 TABLET, FILM COATED in 1 BOTTLE (47335-588-83)
47335-588-8847335058888100 TABLET, FILM COATED in 1 BOTTLE (47335-588-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8bb1965e-7845-4c5b-b021-38e251303d68

Use it

Look up 47335-588 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-588 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-588. 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.