Escitalopram

Product NDC

63629-5349

11-digit product format

636295349

Labeler code

63629

Product ID

63629-5349_a6fdeecb-3f8c-46fd-9228-dddb9ec57b88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA076765

Marketing category

ANDA

Marketing start

2012-03-14

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

2019-12-31

Current FDA listing

Historical FDA.report record