NDC 63187-843 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC63187-843

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
63187-843-3030 TABLET, FILM COATED in 1 BOTTLE (63187-843-30)May 1, 2017
63187-843-6060 TABLET, FILM COATED in 1 BOTTLE (63187-843-60)May 1, 2017
63187-843-9090 TABLET, FILM COATED in 1 BOTTLE (63187-843-90)May 1, 2017

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