NDC 76420-026 – Eszopiclone

Eszopiclone 1 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC76420-026

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202929
Marketed since
January 31, 2015
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (6)

Package NDCDescriptionSince
76420-026-01100 TABLET, FILM COATED in 1 BOTTLE (76420-026-01)Jun 17, 2020
76420-026-1010 TABLET, FILM COATED in 1 BOTTLE (76420-026-10)Jun 17, 2020
76420-026-2020 TABLET, FILM COATED in 1 BOTTLE (76420-026-20)Jun 17, 2020
76420-026-3030 TABLET, FILM COATED in 1 BOTTLE (76420-026-30)Jun 17, 2020
76420-026-6060 TABLET, FILM COATED in 1 BOTTLE (76420-026-60)Jun 17, 2020
76420-026-9090 TABLET, FILM COATED in 1 BOTTLE (76420-026-90)Jun 17, 2020

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