NDC 71335-0512 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC71335-0512

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 (8)

Package NDCDescriptionSince
71335-0512-130 TABLET, FILM COATED in 1 BOTTLE (71335-0512-1)Nov 16, 2015
71335-0512-260 TABLET, FILM COATED in 1 BOTTLE (71335-0512-2)Nov 16, 2015
71335-0512-390 TABLET, FILM COATED in 1 BOTTLE (71335-0512-3)Nov 16, 2015
71335-0512-4120 TABLET, FILM COATED in 1 BOTTLE (71335-0512-4)Nov 16, 2015
71335-0512-520 TABLET, FILM COATED in 1 BOTTLE (71335-0512-5)Nov 16, 2015
71335-0512-6100 TABLET, FILM COATED in 1 BOTTLE (71335-0512-6)Nov 16, 2015
71335-0512-728 TABLET, FILM COATED in 1 BOTTLE (71335-0512-7)Nov 16, 2015
71335-0512-810 TABLET, FILM COATED in 1 BOTTLE (71335-0512-8)Nov 16, 2015

Other Eszopiclone products