NDC 71335-0574 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC71335-0574

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Bryant Ranch Prepack
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 (5)

Package NDCDescriptionSince
71335-0574-130 TABLET, FILM COATED in 1 BOTTLE (71335-0574-1)Jul 17, 2015
71335-0574-260 TABLET, FILM COATED in 1 BOTTLE (71335-0574-2)Jul 17, 2015
71335-0574-390 TABLET, FILM COATED in 1 BOTTLE (71335-0574-3)Jul 17, 2015
71335-0574-410 TABLET, FILM COATED in 1 BOTTLE (71335-0574-4)Jul 17, 2015
71335-0574-5120 TABLET, FILM COATED in 1 BOTTLE (71335-0574-5)Jul 17, 2015

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