United States · FDA National Drug Code directory

ESZOPICLONE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
61919-033_4c47d883-5220-4dd2-e063-6394a90af7a4
Product NDC
61919-033
Form
TABLET, FILM COATED
Composition / generic term
ESZOPICLONE
Labeler
DIRECT RX
Marketing category
ANDA
Marketing start / end (source format)
20170213
Source listing expiry
20271231

Source-listed ingredients

  • ESZOPICLONE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 TABLET, FILM COATED in 1 BOTTLE (61919-033-10) · 61919-033-10
  • 30 TABLET, FILM COATED in 1 BOTTLE (61919-033-30) · 61919-033-30
  • 60 TABLET, FILM COATED in 1 BOTTLE (61919-033-60) · 61919-033-60

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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ESZOPICLONE — United States | Molindra Medicines