NDC 82804-076 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC82804-076

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091166
Marketed since
April 15, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (3)

Package NDCDescriptionSince
82804-076-3030 TABLET, FILM COATED in 1 BOTTLE (82804-076-30)Feb 21, 2024
82804-076-6060 TABLET, FILM COATED in 1 BOTTLE (82804-076-60)Feb 21, 2024
82804-076-9090 TABLET, FILM COATED in 1 BOTTLE (82804-076-90)Feb 21, 2024

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