Escitalopram

Product NDC

59115-100

11-digit product format

591150100

Labeler code

59115

Product ID

59115-100_f69a6fca-cfaf-48d8-86c9-a5ef6bd660ea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Hikma Pharmaceutical

Application

ANDA078766

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record