Escitalopram Oxalate

Product NDC

70518-0972

11-digit product format

705180972

Labeler code

70518

Product ID

70518-0972_8f70068c-10bf-3713-e053-2a95a90a9e93

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA021323

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2018-01-22

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

2020-12-31

Current FDA listing

Historical FDA.report record