NDC 68788-8387 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC68788-8387

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091166
Marketed since
March 1, 2023
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (2)

Package NDCDescriptionSince
68788-8387-330 TABLET, FILM COATED in 1 BOTTLE (68788-8387-3)Mar 1, 2023
68788-8387-660 TABLET, FILM COATED in 1 BOTTLE (68788-8387-6)Mar 1, 2023

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