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Data / Drug companies / Halobetasol propionate

Halobetasol propionate: 11 companies and 17 products in the FDA NDC directory

Halobetasol propionate is listed in the FDA National Drug Code Directory by 11 companies, with 17 products in commercial distribution. 14 of the products (82.4%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are ointment; lotion; cream, and the newest product started marketing on July 1, 2026.

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Companies listing it
11
Products
17
Generic (ANDA) products
14 (82.4%)
Application numbers
9
Routes
Topical
Brand names
Ultravate, Lexette, Bryhali
openFDA record search
api.fda.gov

Companies that list halobetasol propionate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack4ointment; creamGeneric drugs (ANDA)October 6, 2020
Bryant Ranch Prepack2ointmentGeneric drugs (ANDA)February 5, 2009
Cosette Pharmaceuticals, Inc.2ointment; creamGeneric drugs (ANDA)July 16, 2007
Padagis Israel Pharmaceuticals Ltd2cream; ointmentGeneric drugs (ANDA)February 5, 2009
Bausch Health US LLC1lotionNew drug applications (NDA)November 6, 2018
Coral Way Pharma, LLC1lotionAuthorized generics (NDA)March 10, 2026
Encube Ethicals, Inc.1ointmentGeneric drugs (ANDA)July 1, 2026
Lacer Pharma, LLC1lotionNew drug applications (NDA)April 6, 2025
Mayne Pharma1aerosol, foamGeneric drugs (ANDA)November 27, 2023
Mayne Pharma Inc.1aerosol, foamGeneric drugs (ANDA)August 8, 2025
Quagen Pharmaceuticals LLC1ointmentGeneric drugs (ANDA)October 6, 2020

Dosage forms

Dosage formProductsShare
Ointment952.9%
Lotion317.6%
Cream317.6%
Aerosol, foam211.8%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1482.4%
New drug applications (NDA)211.8%
Authorized generics (NDA)15.9%

Pharmacologic classes

ClassProducts
Corticosteroid17

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.