NDC 33342-301 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC33342-301

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Macleods Pharmaceuticals Limited
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
33342-301-11100 TABLET, FILM COATED in 1 BOTTLE (33342-301-11)Jan 31, 2015
33342-301-1210 BLISTER PACK in 1 CARTON (33342-301-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 31, 2015
33342-301-441000 TABLET, FILM COATED in 1 BOTTLE (33342-301-44)Jan 31, 2015

Recalls mentioning this NDC

Other Eszopiclone products