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Data / Drug companies / Alprazolam

Alprazolam: 37 companies and 138 products in the FDA NDC directory

Alprazolam is listed in the FDA National Drug Code Directory by 37 companies, with 138 products in commercial distribution. 112 of the products (81.2%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, extended release; tablet, orally disintegrating, and the newest product started marketing on November 2, 2026.

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Companies listing it
37
Products
138
Generic (ANDA) products
112 (81.2%)
Application numbers
15
Controlled substance schedule
Schedule IV
Routes
Oral
Brand names
Xanax, Xanax XR
openFDA record search
api.fda.gov

Companies that list alprazolam

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack10tablet; tablet, extended releaseGeneric drugs (ANDA)July 31, 2015
Actavis Pharma, Inc.8tablet; tablet, orally disintegratingGeneric drugs (ANDA)March 17, 2010
Asclemed USA, Inc.8tablet, extended release; tabletGeneric drugs (ANDA)June 7, 2011
Aurobindo Pharma Limited8tablet; tablet, extended releaseGeneric drugs (ANDA)July 31, 2015
Mylan Pharmaceuticals Inc.8tablet, extended release; tabletAuthorized generics (NDA)January 17, 2003
NuCare Pharmaceuticals,Inc.7tabletGeneric drugs (ANDA)July 31, 2015
Proficient Rx LP7tablet; tablet, extended releaseGeneric drugs (ANDA)June 7, 2011
Viatris Specialty LLC6tablet; tablet, extended releaseNew drug applications (NDA)October 29, 2025
Advanced Rx of Tennessee, LLC5tabletGeneric drugs (ANDA)November 6, 2024
A-S Medication Solutions4tabletGeneric drugs (ANDA)March 25, 1998
Amneal Pharmaceuticals LLC4tablet, extended releaseGeneric drugs (ANDA)December 3, 2009
Ani Pharmaceuticals, Inc.4tabletGeneric drugs (ANDA)May 11, 2021
Aphena Pharma Solutions - Tennessee, LLC4tabletGeneric drugs (ANDA)December 29, 1995
Asclemed USA Inc.4tabletGeneric drugs (ANDA)July 31, 2015
Clinical Solutions Wholesale, LLC4tabletGeneric drugs (ANDA)July 31, 2015
Natco Pharma USA LLC4tabletGeneric drugs (ANDA)July 28, 2023
Par Health USA, LLC4tablet, orally disintegratingGeneric drugs (ANDA)January 9, 2009
Sandoz Inc4tabletGeneric drugs (ANDA)March 25, 1998
Unichem Pharmaceuticals (USA), Inc.4tabletGeneric drugs (ANDA)November 2, 2026
Aphena Pharma Solutions - Tennessee, LLC3tabletAuthorized generics (NDA)October 16, 1981
AvPAK3tabletGeneric drugs (ANDA)September 25, 2025
PD-Rx Pharmaceuticals, Inc.3tabletGeneric drugs (ANDA)July 31, 2015
Preferred Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)April 7, 2023
Proficient Rx LP3tabletGeneric drugs (ANDA)July 31, 2015
American Health Packaging2tabletGeneric drugs (ANDA)February 7, 2024
Coupler LLC2tabletGeneric drugs (ANDA)May 5, 2026
Proficient Rx LP2tabletAuthorized generics (NDA)October 16, 1981
Bryant Ranch Prepack1tablet, extended releaseGeneric drugs (ANDA)March 12, 2007
Direct_Rx1tabletGeneric drugs (ANDA)March 22, 2023
Hikma Pharmaceuticals USA Inc.1solution, concentrateGeneric drugs (ANDA)October 31, 1993
Medsource Pharmaceuticals1tabletGeneric drugs (ANDA)July 31, 2015
Northwind Health Company, LLC1tabletGeneric drugs (ANDA)August 1, 2024
PD-Rx Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)March 25, 1998
PD-Rx Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)December 29, 1995
Pharmacia & Upjohn Company LLC1tabletNew drug applications (NDA)October 16, 1981
Remedyrepack Inc.1tabletGeneric drugs (ANDA)July 10, 2024
St. Mary's Medical Park Pharmacy1tabletGeneric drugs (ANDA)May 22, 2023

Dosage forms

Dosage formProductsShare
Tablet10576.1%
Tablet, extended release2417.4%
Tablet, orally disintegrating85.8%
Solution, concentrate10.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)11281.2%
Authorized generics (NDA)1913.8%
New drug applications (NDA)75.1%

Pharmacologic classes

ClassProducts
Benzodiazepine138

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.