Escitalopram NDC 51655-449

Product information

Brand name (proprietary)

Escitalopram

Generic name (nonproprietary)

escitalopram

Active ingredients

Escitalopram oxalate — 10 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Northwind Health Company, LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 202389

Marketing start

Oct 20, 2020

Listing expires

Dec 31, 2027

Other FDA classes

Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 51655-449_490edf99-ea97-fea0-e063-6294a90a9e8cSPL ID 490edf99-ea97-fea0-e063-6294a90a9e8cSPL set ID c9f52332-8616-19d8-e053-2995a90ad753RxCUI 349332UNII 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

N451655044952 followed by a unit qualifier and the quantity Copy

Package 51655-0449-52. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 202389

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