Escitalopram

Product NDC

60760-197

11-digit product format

607600197

Labeler code

60760

Product ID

60760-197_7a8dd3fd-e454-02f4-e053-2991aa0a300c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Escitalopram Oxalate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

St. Mary's Medical Park Pharmacy

Application

ANDA202280

Marketing category

ANDA

Marketing start

2014-02-06

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

2019-12-31

Current FDA listing

Historical FDA.report record