Escitalopram

Product NDC

57237-092

11-digit product format

572370092

Labeler code

57237

Product ID

57237-092_12f6a619-58cb-4428-bfa5-66859253efed

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram Oxalate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Citron Pharma LLC

Application

ANDA090432

Marketing category

ANDA

Marketing start

2012-09-11

Marketing end

0000-00-00

Substance

ESCITALOPRAM OXALATE

Active strength

5 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