Escitalopram

Product NDC

68788-9456

11-digit product format

687889456

Labeler code

68788

Product ID

68788-9456_745a1fc2-1e65-475e-8c6f-3dff7ed8ae10

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram Oxalate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA090432

Marketing category

ANDA

Marketing start

2014-09-25

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record