Lexapro

Product NDC

50436-9803

11-digit product format

504369803

Labeler code

50436

Product ID

50436-9803_9270b2e7-ac73-4680-aa5a-00c19c345bca

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ESCITALOPRAM OXALATE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

Application

NDA021323

Marketing category

NDA

Marketing start

2002-08-14

Marketing end

0000-00-00

Substance

ESCITALOPRAM OXALATE

Active strength

10 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record