NDC 68180-323 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC68180-323

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091124
Marketed since
April 15, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (1)

Package NDCDescriptionSince
68180-323-01100 TABLET, FILM COATED in 1 BOTTLE (68180-323-01)Apr 15, 2014

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