Eszopiclone

Product NDC

50090-1899

11-digit product format

500901899

Labeler code

50090

Product ID

50090-1899_2a080e91-ff15-4b02-be41-530009be9f34

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Eszopiclone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA091169

Marketing category

ANDA

Marketing start

2014-04-14

Marketing end

0000-00-00

Substance

ESZOPICLONE

Active strength

1 mg/1

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record