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Data / Drug companies / Fluoxetine

Fluoxetine: 42 companies and 95 products in the FDA NDC directory

Fluoxetine is listed in the FDA National Drug Code Directory by 42 companies, with 95 products in commercial distribution. 95 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; tablet, film coated; tablet, and the newest product started marketing on October 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
42
Products
95
Generic (ANDA) products
95 (100.0%)
Application numbers
18
Routes
Oral
openFDA record search
api.fda.gov

Companies that list fluoxetine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack7capsule; tablet, film coatedGeneric drugs (ANDA)July 11, 2025
Remedyrepack Inc.7capsule; tablet, film coatedGeneric drugs (ANDA)April 23, 2026
Aurobindo Pharma Limited6capsule; tablet, film coatedGeneric drugs (ANDA)July 11, 2025
Alembic Pharmaceuticals Inc.5capsule; tablet, film coatedGeneric drugs (ANDA)April 7, 2017
A-S Medication Solutions4capsuleGeneric drugs (ANDA)September 1, 2025
Alembic Pharmaceuticals Limited3capsuleGeneric drugs (ANDA)July 1, 2009
Aurobindo Pharma Limited3tablet, film coatedGeneric drugs (ANDA)January 15, 2026
BluePoint Laboratories3capsuleGeneric drugs (ANDA)January 8, 2026
Cadila Pharmaceuticals Limited3capsuleGeneric drugs (ANDA)December 15, 2022
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.3capsuleGeneric drugs (ANDA)October 13, 2024
Modavar Pharmaceuticals LLC3capsuleGeneric drugs (ANDA)September 8, 2021
NCS HealthCare of Ky, LLC DBA Vangard Labs3capsuleGeneric drugs (ANDA)July 11, 2025
NorthStar RxLLC3capsuleGeneric drugs (ANDA)September 1, 2025
Bryant Ranch Prepack2tablet, film coatedGeneric drugs (ANDA)November 16, 2017
Coupler LLC2capsuleGeneric drugs (ANDA)October 2, 2026
Legacy Pharmaceutical Packaging, LLC2capsuleGeneric drugs (ANDA)January 25, 2011
NorthStar Rx LLC2tablet, film coatedGeneric drugs (ANDA)September 18, 2019
Northwind Health Company, LLC2capsuleGeneric drugs (ANDA)April 21, 2026
NuCare Pharmaceuticals,Inc.2capsuleGeneric drugs (ANDA)January 29, 2002
PD-Rx Pharmaceuticals, Inc.2capsuleGeneric drugs (ANDA)July 11, 2025
Proficient Rx LP2capsuleGeneric drugs (ANDA)January 30, 2002
QPharma, Inc.2capsuleGeneric drugs (ANDA)July 11, 2025
ScieGen Pharmaceuticals, Inc.2tablet, film coatedGeneric drugs (ANDA)March 20, 2019
Strides Pharma Science Limited2tabletGeneric drugs (ANDA)August 12, 2024
Teva Pharmaceuticals USA, Inc.2capsuleGeneric drugs (ANDA)January 29, 2002
Torrent Pharmaceuticals Limited2tabletGeneric drugs (ANDA)October 21, 2016
Advanced Rx of Tennessee, LLC1capsuleGeneric drugs (ANDA)April 11, 2023
American Health Packaging1solutionGeneric drugs (ANDA)December 4, 2024
American Health Packaging1capsuleGeneric drugs (ANDA)July 14, 2026
Aurobindo Pharma Limited1solutionGeneric drugs (ANDA)March 19, 2009
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)November 16, 2017
Chartwell Governmental & Specialty RX, LLC.1liquidGeneric drugs (ANDA)May 14, 2004
Chartwell RX, LLC1liquidGeneric drugs (ANDA)May 14, 2004
Dr. Reddy's Laboratories Inc.1tablet, film coatedGeneric drugs (ANDA)May 8, 2018
Dr. Reddy's Laboratories Limited1tablet, film coatedGeneric drugs (ANDA)September 30, 2016
PD-Rx Pharmaceuticals, Inc.1capsuleGeneric drugs (ANDA)January 29, 2016
Par Health USA, LLC1tablet, film coatedGeneric drugs (ANDA)November 16, 2017
Preferred Pharmaceuticals Inc.1capsuleGeneric drugs (ANDA)March 28, 2024
Proficient Rx LP1capsuleGeneric drugs (ANDA)January 29, 2002
Saptalis Pharmaceuticals, LLC.1solutionGeneric drugs (ANDA)June 20, 2025
Teva Pharmaceuticals USA, Inc.1capsuleGeneric drugs (ANDA)January 30, 2002
Unit Dose Solutions, Inc.1capsuleGeneric drugs (ANDA)June 22, 2026

Dosage forms

Dosage formProductsShare
Capsule6265.3%
Tablet, film coated2324.2%
Tablet55.3%
Solution33.2%
Liquid22.1%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)95100%

Pharmacologic classes

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