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Data / Drug companies / Olanzapine

Olanzapine: 49 companies and 222 products in the FDA NDC directory

Olanzapine is listed in the FDA National Drug Code Directory by 49 companies, with 222 products in commercial distribution. 208 of the products (93.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, orally disintegrating; tablet, and the newest product started marketing on November 2, 2026.

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Companies listing it
49
Products
222
Generic (ANDA) products
208 (93.7%)
Application numbers
31
Routes
Oral, Intramuscular, Subcutaneous
Brand names
Zyprexa, Zyprexa Zydis, Weltruza, Zyprexa Intramuscular
openFDA record search
api.fda.gov

Companies that list olanzapine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Remedyrepack Inc.15tablet, film coatedGeneric drugs (ANDA)August 19, 2026
Coupler LLC14tablet, film coated; tabletGeneric drugs (ANDA)September 8, 2026
H2-Pharma, LLC11tablet; tablet, orally disintegratingNew drug applications (NDA)April 1, 2004
Apotex Corp.10tablet, film coated; tablet, orally disintegratingGeneric drugs (ANDA)April 23, 2012
Aurobindo Pharma Limited10tablet; tablet, orally disintegratingGeneric drugs (ANDA)May 15, 2014
Hec Pharm USA Inc.10tablet; tablet, orally disintegratingGeneric drugs (ANDA)March 17, 2026
Macleods Pharmaceuticals Limited10tablet, film coated; tablet, orally disintegratingGeneric drugs (ANDA)February 27, 2015
Torrent Pharmaceuticals Limited10tablet; tablet, orally disintegratingGeneric drugs (ANDA)February 28, 2026
Bryant Ranch Prepack7tablet, film coated; tabletGeneric drugs (ANDA)August 22, 2014
Dr. Reddy's Laboratories Limited7tablet, orally disintegrating; tablet, film coatedGeneric drugs (ANDA)April 23, 2012
NorthStar RxLLC7tablet, film coated; injection, powder, for solutionGeneric drugs (ANDA)October 16, 2023
Qilu Pharmaceutical Co., Ltd.7tablet; injection, powder, for solutionGeneric drugs (ANDA)November 11, 2025
Ascend Laboratories, LLC6tabletGeneric drugs (ANDA)January 1, 2012
Cadila Pharmaceuticals Limited6tabletGeneric drugs (ANDA)February 13, 2019
Golden State Medical Supply, Inc.6tablet, film coatedGeneric drugs (ANDA)April 23, 2012
Modavar Pharmaceuticals LLC6tabletGeneric drugs (ANDA)February 27, 2023
American Health Packaging5tablet, film coatedGeneric drugs (ANDA)May 22, 2014
NCS HealthCare of Ky, LLC DBA Vangard Labs5tablet, film coatedGeneric drugs (ANDA)August 22, 2014
Proficient Rx LP5tablet, film coatedGeneric drugs (ANDA)August 22, 2014
Bionpharma Inc.4tablet, orally disintegratingGeneric drugs (ANDA)July 1, 2026
Golden State Medical Supply, Inc.4tablet, orally disintegratingGeneric drugs (ANDA)October 24, 2011
Jubilant Cadista Pharmaceuticals Inc.4tablet, orally disintegratingGeneric drugs (ANDA)September 13, 2012
Lannett Company, Inc.4tablet, orally disintegratingGeneric drugs (ANDA)May 30, 2023
Major Pharmaceuticals4tablet, film coatedGeneric drugs (ANDA)April 23, 2012
Strides Pharma Science Limited4tablet, orally disintegratingGeneric drugs (ANDA)April 11, 2022
Teva Pharmaceuticals USA, Inc.4tablet, orally disintegratingGeneric drugs (ANDA)February 17, 2012
Bryant Ranch Prepack3tablet, orally disintegratingGeneric drugs (ANDA)October 24, 2011
Cardinal Health 107, LLC3tablet, film coatedGeneric drugs (ANDA)July 28, 2026
Dr. Reddy's Laboratories Inc.3tablet, film coatedGeneric drugs (ANDA)December 10, 2013
Preferred Pharmaceuticals Inc.3tablet, film coatedGeneric drugs (ANDA)September 5, 2025
Teva Pharmaceuticals USA, Inc.3kitNew drug applications (NDA)November 2, 2026
Direct_Rx2tablet, film coatedGeneric drugs (ANDA)September 17, 2024
PD-Rx Pharmaceuticals, Inc.2tablet, film coatedGeneric drugs (ANDA)August 22, 2014
Sandoz Inc2injection, powder, for solutionGeneric drugs (ANDA)October 24, 2011
Unit Dose Solutions, Inc.2tablet, film coatedGeneric drugs (ANDA)June 29, 2026
American Regent, Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 27, 2012
Anthea Pharma Private Limited1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)March 5, 2026
Aphena Pharma Solutions - Tennessee, LLC1tablet, film coatedGeneric drugs (ANDA)April 23, 2012
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)August 22, 2014
Camber Pharmaceuticals, Inc.1injection, powder, for solutionGeneric drugs (ANDA)March 22, 2023
Eugia US LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)October 22, 2020
Glenmark Pharmaceuticals Inc., USA1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)March 5, 2026
Hikma Pharmaceuticals USA Inc.1injection, powder, for solutionGeneric drugs (ANDA)September 18, 2025
Pai Holdings, LLC DBA Pai Pharma1injection, powder, for solutionGeneric drugs (ANDA)July 25, 2025
Proficient Rx LP1tablet, film coatedGeneric drugs (ANDA)August 22, 2014
Proficient Rx LP1tablet, film coatedGeneric drugs (ANDA)April 23, 2012
Redpharm Drug1tablet, film coatedGeneric drugs (ANDA)August 22, 2014
Ubi Pharma Inc.1injection, powder, for solutionGeneric drugs (ANDA)May 8, 2020
XGen Pharmaceuticals DJB, Inc.1injection, powder, for solutionGeneric drugs (ANDA)August 28, 2025

Dosage forms

Dosage formProductsShare
Tablet, film coated9542.8%
Tablet, orally disintegrating5725.7%
Tablet5323.9%
Injection, powder, for solution104.5%
Injection, powder, lyophilized, for solution41.8%
Kit31.4%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)20893.7%
New drug applications (NDA)146.3%

Pharmacologic classes

ClassProducts
Atypical Antipsychotic219

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.