Escitalopram Oxalate

Product NDC

51079-544

11-digit product format

510790544

Labeler code

51079

Product ID

51079-544_7be99160-0880-2e07-e053-2a91aa0afa25

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

NDA021323

Marketing category

NDA

Marketing start

2012-02-29

Marketing end

2020-01-31

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

0000-00-00

Current FDA listing

Historical FDA.report record