NDC 71205-236 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC71205-236

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208451
Marketed since
September 15, 2016
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (3)

Package NDCDescriptionSince
71205-236-3030 TABLET, FILM COATED in 1 BOTTLE (71205-236-30)Mar 1, 2019
71205-236-6060 TABLET, FILM COATED in 1 BOTTLE (71205-236-60)Mar 1, 2019
71205-236-9090 TABLET, FILM COATED in 1 BOTTLE (71205-236-90)Mar 1, 2019

Other Eszopiclone products