NDC 76420-353 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC76420-353

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091166
Marketed since
April 15, 2014
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (5)

Package NDCDescriptionSince
76420-353-001000 TABLET, FILM COATED in 1 BOTTLE (76420-353-00)May 22, 2025
76420-353-01100 TABLET, FILM COATED in 1 BOTTLE (76420-353-01)May 22, 2025
76420-353-3030 TABLET, FILM COATED in 1 BOTTLE (76420-353-30)May 22, 2025
76420-353-6060 TABLET, FILM COATED in 1 BOTTLE (76420-353-60)May 22, 2025
76420-353-9090 TABLET, FILM COATED in 1 BOTTLE (76420-353-90)May 22, 2025

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