NDC 71335-9659 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC71335-9659

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208451
Marketed since
September 15, 2016
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (6)

Package NDCDescriptionSince
71335-9659-130 TABLET, FILM COATED in 1 BOTTLE (71335-9659-1)Feb 27, 2023
71335-9659-260 TABLET, FILM COATED in 1 BOTTLE (71335-9659-2)Feb 27, 2023
71335-9659-390 TABLET, FILM COATED in 1 BOTTLE (71335-9659-3)Feb 27, 2023
71335-9659-410 TABLET, FILM COATED in 1 BOTTLE (71335-9659-4)Feb 27, 2023
71335-9659-5120 TABLET, FILM COATED in 1 BOTTLE (71335-9659-5)Feb 27, 2023
71335-9659-6100 TABLET, FILM COATED in 1 BOTTLE (71335-9659-6)Feb 27, 2023

Other Eszopiclone products