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ESZOPICLONE

NDC 72789-067 · PD-Rx Pharmaceuticals, Inc.

Generic nameESZOPICLONE

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ESZOPICLONE

Strength3 mg/1

DEA scheduleCIV

Marketing categoryANDA

Packages

72789-067-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-067-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-0089 — Eszopiclone, 71335-0116 — Eszopiclone, 71335-0512 — Eszopiclone, 71335-0574 — Eszopiclone, 71335-0598 — Eszopiclone, 71335-2002 — Eszopiclone, 71335-2698 — Eszopiclone, 71335-9659 — ESZOPICLONE, 71610-409 — Eszopiclone, 72189-099 — ESZOPICLONE, 76420-024 — Eszopiclone, 76420-026 — Eszopiclone, 76420-027 — Eszopiclone, 76420-352 — Eszopiclone, 76420-353 — Eszopiclone, 76420-354 — Eszopiclone, 80425-0062 — Eszopiclone, 80425-0063 — Eszopiclone, 80425-0064 — Eszopiclone, 80425-0065 — 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