Eszopiclone

Product NDC

70518-0888

11-digit product format

705180888

Labeler code

70518

Product ID

70518-0888_8f05fb54-a9ea-8925-e053-2995a90a8e03

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Eszopiclone

Dosage form

TABLET, FILM COATED

Route

OROPHARYNGEAL

Labeler

REMEDYREPACK INC.

Application

ANDA091166

Marketing category

ANDA

Marketing start

2017-12-05

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