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Data / Drug companies / Escitalopram oxalate

Escitalopram oxalate: 22 companies and 50 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Escitalopram oxalate is listed in the FDA National Drug Code Directory by 22 companies, with 50 products in commercial distribution. 50 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; solution, and the newest product started marketing on March 13, 2024.

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Companies listing it
22
Products
50
Generic (ANDA) products
50 (100.0%)
Application numbers
7
Routes
Oral
Brand names
Escitalopram
openFDA record search
api.fda.gov

Companies that list escitalopram oxalate

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions4tablet, film coatedGeneric drugs (ANDA)January 8, 2024
Aurobindo Pharma Limited4tablet, film coated; solutionGeneric drugs (ANDA)September 11, 2012
Proficient Rx LP4tablet, film coated; tabletGeneric drugs (ANDA)September 11, 2012
Amneal Pharmaceuticals LLC3tablet, film coatedGeneric drugs (ANDA)May 17, 2017
Amneal Pharmaceuticals of New York LLC3tablet, film coatedGeneric drugs (ANDA)May 17, 2017
Asclemed USA, Inc.3tablet, film coatedGeneric drugs (ANDA)September 11, 2012
Bryant Ranch Prepack3tablet, film coated; tabletGeneric drugs (ANDA)September 11, 2012
Jubilant Cadista Pharmaceuticals Inc.3tablet, film coatedGeneric drugs (ANDA)January 1, 2024
Macleods Pharmaceuticals Limited3tablet, film coatedGeneric drugs (ANDA)September 11, 2012
NCS HealthCare of Ky, LLC DBA Vangard Labs3tablet, film coatedGeneric drugs (ANDA)September 11, 2012
NorthStar RxLLC3tablet, film coatedGeneric drugs (ANDA)January 8, 2024
Quallent Pharmaceuticals Health LLC3tabletGeneric drugs (ANDA)March 1, 2023
American Health Packaging2tablet, film coatedGeneric drugs (ANDA)October 8, 2012
Advanced Rx of Tennessee, LLC1tablet, film coatedGeneric drugs (ANDA)March 13, 2024
Camber Pharmaceuticals, Inc.1solutionGeneric drugs (ANDA)June 12, 2012
Northwind Health Company, LLC1tablet, film coatedGeneric drugs (ANDA)January 25, 2023
PD-Rx Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)September 11, 2012
PD-Rx Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)September 11, 2012
Preferred Pharmaceuticals Inc.1tablet, film coatedGeneric drugs (ANDA)February 1, 2023
QPharma, Inc.1tablet, film coatedGeneric drugs (ANDA)September 11, 2012
Rising Pharma Holdings, Inc.1solutionGeneric drugs (ANDA)April 3, 2012
St. Mary's Medical Park Pharmacy1tablet, film coatedGeneric drugs (ANDA)October 24, 2023

Dosage forms

Dosage formProductsShare
Tablet, film coated4182%
Tablet612%
Solution36%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)50100%

Pharmacologic classes

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.