NDC 68462-382 – Eszopiclone

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

Human Prescription Drug DEA schedule CIV

Product NDC68462-382

Product details

Brand name
Eszopiclone
Generic name
Eszopiclone
Labeler
Glenmark Pharmaceuticals Inc. USA
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091166
Marketed since
April 15, 2014
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eszopiclone →

Package NDC codes (3)

Package NDCDescriptionSince
68462-382-01100 TABLET, FILM COATED in 1 BOTTLE (68462-382-01)Apr 15, 2014
68462-382-101000 TABLET, FILM COATED in 1 BOTTLE (68462-382-10)Apr 15, 2014
68462-382-3030 TABLET, FILM COATED in 1 BOTTLE (68462-382-30)Apr 15, 2014

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