NDC 71335-0598 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC71335-0598

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 (6)

Package NDCDescriptionSince
71335-0598-130 TABLET, FILM COATED in 1 BOTTLE (71335-0598-1)Nov 21, 2017
71335-0598-260 TABLET, FILM COATED in 1 BOTTLE (71335-0598-2)Nov 21, 2017
71335-0598-390 TABLET, FILM COATED in 1 BOTTLE (71335-0598-3)Nov 21, 2017
71335-0598-410 TABLET, FILM COATED in 1 BOTTLE (71335-0598-4)Nov 21, 2017
71335-0598-5120 TABLET, FILM COATED in 1 BOTTLE (71335-0598-5)Nov 21, 2017
71335-0598-6100 TABLET, FILM COATED in 1 BOTTLE (71335-0598-6)Nov 21, 2017

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