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Data / Drug companies / Tolterodine tartrate

Tolterodine tartrate: 13 companies and 29 products in the FDA NDC directory

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

Tolterodine tartrate is listed in the FDA National Drug Code Directory by 13 companies, with 29 products in commercial distribution. 28 of the products (96.6%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule, extended release; tablet, film coated; tablet, and the newest product started marketing on June 24, 2026.

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Companies listing it
13
Products
29
Generic (ANDA) products
28 (96.6%)
Application numbers
12
Routes
Oral
Brand names
Detrol
openFDA record search
api.fda.gov

Companies that list tolterodine tartrate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Camber Pharmaceuticals, Inc.4capsule, extended release; tablet, film coatedGeneric drugs (ANDA)August 2, 2021
Teva Pharmaceuticals USA, Inc.4capsule, extended release; tablet, film coatedGeneric drugs (ANDA)March 20, 2017
Unichem Pharmaceuticals (USA), Inc.4capsule, extended release; tabletGeneric drugs (ANDA)October 1, 2024
Ajanta Pharma USA Inc.2capsule, extended releaseGeneric drugs (ANDA)June 25, 2020
Ani Pharmaceuticals, Inc.2capsule, extended releaseGeneric drugs (ANDA)August 29, 2019
Golden State Medical Supply, Inc.2capsule, extended releaseGeneric drugs (ANDA)August 19, 2019
Macleods Pharmaceuticals Limited2tablet, film coatedGeneric drugs (ANDA)October 8, 2020
Major Pharmaceuticals2capsule, extended releaseGeneric drugs (ANDA)June 24, 2026
Rising Pharma Holdings, Inc.2tablet, film coatedGeneric drugs (ANDA)January 24, 2020
Slate Run Pharmaceuticals, LLC2capsule, extended releaseGeneric drugs (ANDA)April 12, 2021
A-S Medication Solutions1capsule, extended releaseGeneric drugs (ANDA)March 20, 2017
Proficient Rx LP1tablet, film coatedGeneric drugs (ANDA)November 1, 2015
Viatris Specialty LLC1tablet, film coatedNew drug applications (NDA)August 1, 2024

Dosage forms

Dosage formProductsShare
Capsule, extended release1758.6%
Tablet, film coated1034.5%
Tablet26.9%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)2896.6%
New drug applications (NDA)13.4%

Pharmacologic classes

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.