NDC 76420-024 – Eszopiclone

Eszopiclone 2 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC76420-024

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
76420-024-01100 TABLET, FILM COATED in 1 BOTTLE (76420-024-01)Jun 17, 2020
76420-024-1010 TABLET, FILM COATED in 1 BOTTLE (76420-024-10)Jun 17, 2020
76420-024-2020 TABLET, FILM COATED in 1 BOTTLE (76420-024-20)Jun 17, 2020
76420-024-3030 TABLET, FILM COATED in 1 BOTTLE (76420-024-30)Jun 17, 2020
76420-024-6060 TABLET, FILM COATED in 1 BOTTLE (76420-024-60)Jun 17, 2020
76420-024-9090 TABLET, FILM COATED in 1 BOTTLE (76420-024-90)Jun 17, 2020

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