NDC 71335-0089 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC71335-0089

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Bryant Ranch Prepack
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 (8)

Package NDCDescriptionSince
71335-0089-130 TABLET, FILM COATED in 1 BOTTLE (71335-0089-1)Feb 7, 2017
71335-0089-260 TABLET, FILM COATED in 1 BOTTLE (71335-0089-2)Feb 7, 2017
71335-0089-390 TABLET, FILM COATED in 1 BOTTLE (71335-0089-3)Feb 7, 2017
71335-0089-4120 TABLET, FILM COATED in 1 BOTTLE (71335-0089-4)Feb 7, 2017
71335-0089-520 TABLET, FILM COATED in 1 BOTTLE (71335-0089-5)Feb 7, 2017
71335-0089-6100 TABLET, FILM COATED in 1 BOTTLE (71335-0089-6)Feb 7, 2017
71335-0089-728 TABLET, FILM COATED in 1 BOTTLE (71335-0089-7)Feb 7, 2017
71335-0089-810 TABLET, FILM COATED in 1 BOTTLE (71335-0089-8)Feb 7, 2017

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