escitalopram NDC 16571-756

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

Rising Pharma Holdings, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 078777

Marketing start

Jun 10, 2023

Listing expires

Dec 31, 2026

Other FDA classes

Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 16571-756_9929f3a5-d78b-4d99-bf87-d2693a9ac47eSPL ID 9929f3a5-d78b-4d99-bf87-d2693a9ac47eSPL set ID ccbe97b5-da68-4fff-929a-240dd705fe6fRxCUI 349332, 351249, 351250UNII 5U85DBW7LOUPC 0316571756018

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

N416571075601 followed by a unit qualifier and the quantity Copy

Package 16571-0756-01. 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

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

Other NDCs under ANDA 078777

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