NDC 69452-349 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC69452-349

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Bionpharma Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091113
Marketed since
June 1, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (1)

Package NDCDescriptionSince
69452-349-20100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-349-20)Jun 1, 2022

Other Eszopiclone products