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Data / Drug companies / Oxymorphone hydrochloride

Oxymorphone hydrochloride: 9 companies and 27 products in the FDA NDC directory

Oxymorphone hydrochloride is listed in the FDA National Drug Code Directory by 9 companies, with 27 products in commercial distribution. 27 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, extended release; tablet, and the newest product started marketing on May 6, 2020.

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Companies listing it
9
Products
27
Generic (ANDA) products
27 (100.0%)
Application numbers
6
Controlled substance schedule
Schedule II
Routes
Oral
openFDA record search
api.fda.gov

Companies that list oxymorphone hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Amneal Pharmaceuticals LLC7tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Amneal Pharmaceuticals of New York LLC7tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Aurolife Pharma, LLC2tabletGeneric drugs (ANDA)April 26, 2016
Camber Pharmaceuticals, Inc.2tabletGeneric drugs (ANDA)March 1, 2018
Epic Pharma, LLC2tabletGeneric drugs (ANDA)May 15, 2019
Hikma Pharmaceuticals USA Inc.2tabletGeneric drugs (ANDA)September 27, 2010
KVK-Tech, Inc.2tabletGeneric drugs (ANDA)February 11, 2013
XLCare Pharmaceuticals, Inc.2tabletGeneric drugs (ANDA)May 6, 2020
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)March 1, 2018

Dosage forms

Dosage formProductsShare
Tablet, film coated, extended release1451.9%
Tablet1348.1%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)27100%

Pharmacologic classes

ClassProducts
Opioid Agonist27

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.