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Data / Drug companies / Oxybutynin

Oxybutynin: 6 companies and 12 products in the FDA NDC directory

Oxybutynin is listed in the FDA National Drug Code Directory by 6 companies, with 12 products in commercial distribution. 10 of the products (83.3%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated, extended release; patch, and the newest product started marketing on August 10, 2017.

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Companies listing it
6
Products
12
Generic (ANDA) products
10 (83.3%)
Application numbers
3
Routes
Oral, Transdermal
Brand names
Oxytrol, Oxytrol for Women
openFDA record search
api.fda.gov

Companies that list oxybutynin

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Zydus Lifesciences Limited3tablet, film coated, extended releaseGeneric drugs (ANDA)August 10, 2017
Zydus Pharmaceuticals USA Inc.3tablet, film coated, extended releaseGeneric drugs (ANDA)August 10, 2017
Allergan, Inc.2patchNew drug applications (NDA)January 1, 2016
NCS HealthCare of Ky, LLC DBA Vangard Labs2tablet, film coated, extended releaseGeneric drugs (ANDA)August 10, 2017
A-S Medication Solutions1tablet, film coated, extended releaseGeneric drugs (ANDA)August 10, 2017
Redpharm Drug1tablet, film coated, extended releaseGeneric drugs (ANDA)August 10, 2017

Dosage forms

Dosage formProductsShare
Tablet, film coated, extended release1083.3%
Patch216.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1083.3%
New drug applications (NDA)216.7%

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.