Escitalopram (escitalopram oxalate) NDC 76420-721

Product information

Brand name (proprietary)

Escitalopram

Generic name (nonproprietary)

escitalopram oxalate

Active ingredients

Escitalopram oxalate — 5 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Asclemed USA, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 090432

Marketing start

Sep 11, 2012

Listing expires

Dec 31, 2027

Other FDA classes

Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 76420-721_4ac15baa-6fcc-476b-e063-6294a90a2a89SPL ID 4ac15baa-6fcc-476b-e063-6294a90a2a89SPL set ID 2957a003-7714-4e16-aeca-623fd6c5d702RxCUI 349332, 351249, 351250UNII 5U85DBW7LO

Pharmacologic class

Serotonin Reuptake Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N476420072101 followed by a unit qualifier and the quantity Copy

Package 76420-0721-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under ANDA 090432

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.