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Data / Drug companies / Terbinafine hydrochloride

Terbinafine hydrochloride: 39 companies and 63 products in the FDA NDC directory

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

Terbinafine hydrochloride is listed in the FDA National Drug Code Directory by 39 companies, with 63 products in commercial distribution. 55 of the products (87.3%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are cream; tablet; spray, and the newest product started marketing on March 1, 2026.

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Companies listing it
39
Products
63
Generic (ANDA) products
55 (87.3%)
Application numbers
9
Routes
Topical, Oral
Brand names
Terbinafine, Lamisil at Cream, Athletes Foot, Lamisil at, Good Neighbor Pharmacy, Antifungal, Silka Jock Itch, Athlete Foot Cream
openFDA record search
api.fda.gov

Companies that list terbinafine hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions6tablet; creamGeneric drugs (ANDA)January 28, 2022
Karo Healthcare Inc.5cream; sprayNew drug applications (NDA)December 10, 2025
Bryant Ranch Prepack3tabletGeneric drugs (ANDA)January 28, 2022
NuCare Pharmaceuticals,Inc.3tabletGeneric drugs (ANDA)August 13, 2014
Preferred Pharmaceuticals Inc.3cream; tabletGeneric drugs (ANDA)October 17, 2025
Proficient Rx LP3tabletGeneric drugs (ANDA)December 27, 2010
Bryant Ranch Prepack2tabletGeneric drugs (ANDA)December 27, 2010
CVS Pharmacy2creamGeneric drugs (ANDA)July 2, 2007
Genomma Lab USA2creamGeneric drugs (ANDA)July 2, 2007
Remedyrepack Inc.2tabletGeneric drugs (ANDA)November 3, 2023
Sun Pharmaceutical Industries, Inc.2creamGeneric drugs (ANDA)July 2, 2007
Voyant Beauty, Inc.2creamNew drug applications (NDA)August 21, 2024
Walgreen Company2creamGeneric drugs (ANDA)October 25, 2023
American Health Packaging1tabletGeneric drugs (ANDA)March 1, 2026
Amerisource Bergen1creamGeneric drugs (ANDA)July 2, 2007
Aphena Pharma Solutions - Tennessee, LLC1tabletGeneric drugs (ANDA)August 22, 2012
Aurobindo Pharma Limited1tabletGeneric drugs (ANDA)July 2, 2007
Beautivity LLC1creamOver the counter monograph drugsAugust 18, 2025
Bionpharma Inc.1tabletGeneric drugs (ANDA)January 28, 2022
Breckenridge Pharmaceutical, Inc.1tabletGeneric drugs (ANDA)December 27, 2010
Cardinal Health 110, LLC. DBA Leader1creamGeneric drugs (ANDA)July 30, 2018
Dr. Reddy's Laboratories Limited1tabletGeneric drugs (ANDA)July 2, 2007
Golden State Medical Supply, Inc.1tabletGeneric drugs (ANDA)June 4, 2010
H E B1creamGeneric drugs (ANDA)July 2, 2007
Kroger Company1creamGeneric drugs (ANDA)July 2, 2007
Little Pharma, Inc.1creamGeneric drugs (ANDA)December 10, 2024
Meijer Distribution Inc1creamGeneric drugs (ANDA)July 2, 2007
NorthStar Rx LLC1tabletGeneric drugs (ANDA)July 2, 2007
Northwind Health Company, LLC1tabletGeneric drugs (ANDA)May 28, 2020
PD-Rx Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)December 27, 2010
PD-Rx Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)July 2, 2007
Proficient Rx LP1tabletGeneric drugs (ANDA)January 28, 2022
Proficient Rx LP1creamGeneric drugs (ANDA)July 2, 2007
Publix Super Markets Inc1creamGeneric drugs (ANDA)July 2, 2007
Rite Aid Corporation1creamGeneric drugs (ANDA)July 2, 2007
Scholls Wellness Company LLC1creamGeneric drugs (ANDA)September 11, 2025
Sportpharm LLC1creamGeneric drugs (ANDA)July 2, 2007
Strategic Sourcing Services LLC1creamGeneric drugs (ANDA)June 30, 2023
Wal-Mart Stores Inc1creamGeneric drugs (ANDA)July 2, 2007

Dosage forms

Dosage formProductsShare
Cream3149.2%
Tablet3047.6%
Spray23.2%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)5587.3%
New drug applications (NDA)711.1%
Over the counter monograph drugs11.6%

Pharmacologic classes

ClassProducts
Allylamine Antifungal63

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.