NDC 68788-7169 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC68788-7169

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
June 11, 2018
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (5)

Package NDCDescriptionSince
68788-7169-110 TABLET, FILM COATED in 1 BOTTLE (68788-7169-1)Jun 11, 2018
68788-7169-220 TABLET, FILM COATED in 1 BOTTLE (68788-7169-2)Jun 11, 2018
68788-7169-330 TABLET, FILM COATED in 1 BOTTLE (68788-7169-3)Jun 11, 2018
68788-7169-660 TABLET, FILM COATED in 1 BOTTLE (68788-7169-6)Jun 11, 2018
68788-7169-990 TABLET, FILM COATED in 1 BOTTLE (68788-7169-9)Jun 11, 2018

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