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Data / Drug companies / Flavoxate hydrochloride

Flavoxate hydrochloride: 3 companies and 3 products in the FDA NDC directory

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

Flavoxate hydrochloride is listed in the FDA National Drug Code Directory by 3 companies, with 3 products in commercial distribution. 3 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated, and the newest product started marketing on December 15, 2016.

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Companies listing it
3
Products
3
Generic (ANDA) products
3 (100.0%)
Application numbers
2
Routes
Oral
openFDA record search
api.fda.gov

Companies that list flavoxate hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Epic Pharma, LLC1tabletGeneric drugs (ANDA)February 21, 2011
Padagis US LLC1tablet, film coatedGeneric drugs (ANDA)December 22, 2004
Puracap Laboratories LLC DBA Blu Pharmaceuticals1tabletGeneric drugs (ANDA)December 15, 2016

Dosage forms

Dosage formProductsShare
Tablet266.7%
Tablet, film coated133.3%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)3100%

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.