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Eszopiclone

NDC 70518-4398 · REMEDYREPACK INC.

Generic nameEszopiclone

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ESZOPICLONE

Strength2 mg/1

DEA scheduleCIV

Marketing categoryANDA

Packages

70518-4398-0 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4398-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-7169 — Eszopiclone, 68788-7667 — ESZOPICLONE, 68788-8387 — Eszopiclone, 68788-8826 — Eszopiclone, 69452-347 — ESZOPICLONE, 69452-348 — ESZOPICLONE, 69452-349 — ESZOPICLONE, 70518-1310 — ESZOPICLONE, 70518-3576 — Eszopiclone, 70518-4361 — Eszopiclone, 71205-236 — ESZOPICLONE, 71205-384 — ESZOPICLONE, 71205-513 — ESZOPICLONE, 71205-581 — Eszopiclone, 71205-633 — Eszopiclone, 71335-0089 — Eszopiclone, 71335-0116 — Eszopiclone, 71335-0512 — Eszopiclone, 71335-0574 — Eszopiclone, 71335-0598 — Eszopiclone, +73 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels