NDC 63187-817 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC63187-817

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Proficient Rx LP
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 (3)

Package NDCDescriptionSince
63187-817-3030 TABLET, FILM COATED in 1 BOTTLE (63187-817-30)Feb 1, 2017
63187-817-6060 TABLET, FILM COATED in 1 BOTTLE (63187-817-60)Feb 1, 2017
63187-817-9090 TABLET, FILM COATED in 1 BOTTLE (63187-817-90)Feb 1, 2017

Other Eszopiclone products