NDC 0093-5539 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC0093-5539

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091169
Marketed since
April 14, 2014
Marketing end
February 28, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (1)

Package NDCDescriptionSince
0093-5539-01100 TABLET, FILM COATED in 1 BOTTLE (0093-5539-01)Apr 14, 2014

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