NDC 71205-384 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC71205-384

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
71205-384-3030 TABLET, FILM COATED in 1 BOTTLE (71205-384-30)Jan 10, 2020
71205-384-6060 TABLET, FILM COATED in 1 BOTTLE (71205-384-60)Jan 10, 2020
71205-384-9090 TABLET, FILM COATED in 1 BOTTLE (71205-384-90)Jan 10, 2020

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