NDC 68788-7029 – Eszopiclone

Eszopiclone 2 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC68788-7029

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202929
Marketed since
October 12, 2017
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (5)

Package NDCDescriptionSince
68788-7029-110 TABLET, FILM COATED in 1 BOTTLE (68788-7029-1)Oct 12, 2017
68788-7029-220 TABLET, FILM COATED in 1 BOTTLE (68788-7029-2)Oct 12, 2017
68788-7029-330 TABLET, FILM COATED in 1 BOTTLE (68788-7029-3)Oct 12, 2017
68788-7029-660 TABLET, FILM COATED in 1 BOTTLE (68788-7029-6)Oct 12, 2017
68788-7029-990 TABLET, FILM COATED in 1 BOTTLE (68788-7029-9)Oct 12, 2017

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