Escitalopram

Product NDC

43063-521

11-digit product format

430630521

Labeler code

43063

Product ID

43063-521_a8db0b3a-d44b-f640-e053-2a95a90a1829

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

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

2021-12-31

Current FDA listing

Historical FDA.report record