Escitalopram

Product NDC

55700-157

11-digit product format

557000157

Labeler code

55700

Product ID

55700-157_960d3aa0-ebac-421b-b01f-07ad58d3cf57

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076765

Marketing category

ANDA

Marketing start

2012-03-14

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