escitalopram

Product NDC

54879-011

11-digit product format

548790011

Labeler code

54879

Product ID

54879-011_b33ea9f7-1fa9-4ba8-8a3c-6f9897015044

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

STI Pharma LLC

Application

ANDA077512

Marketing category

ANDA

Marketing start

2013-09-12

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