Escitalopram

Product NDC

43063-389

11-digit product format

430630389

Labeler code

43063

Product ID

43063-389_7d3f2efb-bb38-26b3-e053-2a91aa0a2d56

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA078766

Marketing category

ANDA

Marketing start

2012-09-11

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

2019-12-31

Current FDA listing

Historical FDA.report record