NDC 31722-857 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC31722-857

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205504
Marketed since
January 4, 2024
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (2)

Package NDCDescriptionSince
31722-857-01100 TABLET, FILM COATED in 1 BOTTLE (31722-857-01)Jan 4, 2024
31722-857-3030 TABLET, FILM COATED in 1 BOTTLE (31722-857-30)Jan 4, 2024

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