NDC 82804-159 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC82804-159

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205504
Marketed since
January 4, 2024
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (3)

Package NDCDescriptionSince
82804-159-3030 TABLET, FILM COATED in 1 BOTTLE (82804-159-30)Feb 6, 2026
82804-159-6060 TABLET, FILM COATED in 1 BOTTLE (82804-159-60)Mar 12, 2025
82804-159-9090 TABLET, FILM COATED in 1 BOTTLE (82804-159-90)Oct 11, 2024

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