Escitalopram Oxalate

Product NDC

67046-173

11-digit product format

670460173

Labeler code

67046

Product ID

67046-173_5a058aa9-323a-4ce6-e053-2991aa0a90ea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

escitalopram

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Contract Pharmacy Services-PA

Application

NDA021323

Marketing category

NDA

Marketing start

2017-09-25

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