Eszopiclone

Product NDC

50436-5539

11-digit product format

504365539

Labeler code

50436

Product ID

50436-5539_217153c5-d085-43a3-92a8-5b2cbda2dbd6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Eszopiclone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA091169

Marketing category

ANDA

Marketing start

2014-04-14

Marketing end

0000-00-00

Substance

ESZOPICLONE

Active strength

3 mg/1

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record