Escitalopram

Product NDC

70518-0692

11-digit product format

705180692

Labeler code

70518

Product ID

70518-0692_8ac60e30-4b54-64cd-e053-2995a90ab656

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076765

Marketing category

ANDA

Marketing start

2017-08-17

Marketing end

0000-00-00

Substance

ESCITALOPRAM OXALATE

Active strength

10 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