ESZOPICLONE

Product NDC

68788-9824

11-digit product format

687889824

Labeler code

68788

Product ID

68788-9824_1647c3bf-1211-4d78-b0c5-cd86a66df134

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ESZOPICLONE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA091103

Marketing category

ANDA

Marketing start

2015-08-18

Marketing end

0000-00-00

Substance

ESZOPICLONE

Active strength

3 mg/1

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record