Escitalopram

Product NDC

0615-7722

11-digit product format

006157722

Labeler code

0615

Product ID

0615-7722_2b4cd7d7-bdf7-4e7d-aeb5-d6d6fe04d8cc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record