Escitalopram

Product NDC

0143-9807

11-digit product format

001439807

Labeler code

0143

Product ID

0143-9807_322655e3-fff3-4292-abf5-fb9634227072

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

West-Ward Pharmaceuticals Corp

Application

ANDA078766

Marketing category

ANDA

Marketing start

2012-09-11

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