Escitalopram

Product NDC

50090-2699

11-digit product format

500902699

Labeler code

50090

Product ID

50090-2699_5c7610ea-5645-4245-a448-9a4c0a11c92d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA202389

Marketing category

ANDA

Marketing start

2013-03-21

Marketing end

0000-00-00

Substance

ESCITALOPRAM OXALATE

Active strength

20 mg/1

Pharmacologic classes

Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record