NDC 71205-581 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC71205-581

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091166
Marketed since
April 15, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (3)

Package NDCDescriptionSince
71205-581-3030 TABLET, FILM COATED in 1 BOTTLE (71205-581-30)Jun 23, 2021
71205-581-6060 TABLET, FILM COATED in 1 BOTTLE (71205-581-60)Jun 23, 2021
71205-581-9090 TABLET, FILM COATED in 1 BOTTLE (71205-581-90)Jun 23, 2021

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