NDC 47335-586 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC47335-586

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091103
Marketed since
April 15, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (4)

Package NDCDescriptionSince
47335-586-08100 TABLET, FILM COATED in 1 BOTTLE (47335-586-08)Apr 15, 2014
47335-586-181000 TABLET, FILM COATED in 1 BOTTLE (47335-586-18)Apr 15, 2014
47335-586-8330 TABLET, FILM COATED in 1 BOTTLE (47335-586-83)Apr 15, 2014
47335-586-88100 TABLET, FILM COATED in 1 BOTTLE (47335-586-88)Apr 15, 2014

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