NDC 68788-7667 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC68788-7667

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208451
Marketed since
February 28, 2020
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (8)

Package NDCDescriptionSince
68788-7667-0100 TABLET, FILM COATED in 1 BOTTLE (68788-7667-0)Feb 28, 2020
68788-7667-110 TABLET, FILM COATED in 1 BOTTLE (68788-7667-1)Feb 28, 2020
68788-7667-220 TABLET, FILM COATED in 1 BOTTLE (68788-7667-2)Feb 28, 2020
68788-7667-330 TABLET, FILM COATED in 1 BOTTLE (68788-7667-3)Feb 28, 2020
68788-7667-515 TABLET, FILM COATED in 1 BOTTLE (68788-7667-5)Feb 28, 2020
68788-7667-660 TABLET, FILM COATED in 1 BOTTLE (68788-7667-6)Feb 28, 2020
68788-7667-77 TABLET, FILM COATED in 1 BOTTLE (68788-7667-7)Feb 28, 2020
68788-7667-990 TABLET, FILM COATED in 1 BOTTLE (68788-7667-9)Feb 28, 2020

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