ESZOPICLONE

Product NDC

68788-8953

11-digit product format

687888953

Labeler code

68788

Product ID

68788-8953_e5048d9d-09e7-4c55-acc1-cfb1460bffb1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ESZOPICLONE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA091113

Marketing category

ANDA

Marketing start

2015-11-20

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