Eszopiclone

Product NDC

51079-414

11-digit product format

510790414

Labeler code

51079

Product ID

51079-414_9b048684-a408-13a5-e053-2a95a90a6e9d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

eszopiclone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA091151

Marketing category

ANDA

Marketing start

2014-11-11

Marketing end

2020-10-31

Substance

ESZOPICLONE

Active strength

3 mg/1

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record