NDC 71335-0116 – Eszopiclone

Eszopiclone 3 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-0116

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
April 25, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (8)

Package NDCDescriptionSince
71335-0116-130 TABLET, FILM COATED in 1 BOTTLE (71335-0116-1)Jan 24, 2017
71335-0116-260 TABLET, FILM COATED in 1 BOTTLE (71335-0116-2)Jan 24, 2017
71335-0116-390 TABLET, FILM COATED in 1 BOTTLE (71335-0116-3)Jan 24, 2017
71335-0116-4120 TABLET, FILM COATED in 1 BOTTLE (71335-0116-4)Jan 24, 2017
71335-0116-520 TABLET, FILM COATED in 1 BOTTLE (71335-0116-5)Jan 24, 2017
71335-0116-628 TABLET, FILM COATED in 1 BOTTLE (71335-0116-6)Jan 24, 2017
71335-0116-715 TABLET, FILM COATED in 1 BOTTLE (71335-0116-7)Jan 24, 2017
71335-0116-8100 TABLET, FILM COATED in 1 BOTTLE (71335-0116-8)Jan 24, 2017

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