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Data / Drug companies / Diclofenac epolamine

Diclofenac epolamine: 11 companies and 14 products in the FDA NDC directory

Diclofenac epolamine is listed in the FDA National Drug Code Directory by 11 companies, with 14 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are system, and the newest product started marketing on June 8, 2026.

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Companies listing it
11
Products
14
Generic (ANDA) products
0 (0.0%)
Application numbers
2
Routes
Topical
Brand names
Licart, Flector
openFDA record search
api.fda.gov

Companies that list diclofenac epolamine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Advanced Rx of Tennessee, LLC2systemAuthorized generics (NDA)June 19, 2024
Asclemed USA, Inc.2systemAuthorized generics (NDA)November 18, 2022
Ibsa Pharma Inc.2systemNew drug applications (NDA)November 1, 2020
Acertis Pharmaceuticals, LLC1systemNew drug applications (NDA)September 1, 2020
Hawaii Repack, Inc.1systemAuthorized generics (NDA)November 18, 2022
Phoenix RX LLC1systemAuthorized generics (NDA)November 18, 2022
Preferred Pharmaceuticals Inc.1systemAuthorized generics (NDA)June 8, 2026
Quality Care Products, LLC1systemAuthorized generics (NDA)August 15, 2023
Sportpharm LLC1systemAuthorized generics (NDA)November 18, 2022
Teva Pharmaceuticals USA, Inc.1systemAuthorized generics (NDA)May 1, 2020
Yaral Pharma Inc.1systemAuthorized generics (NDA)November 18, 2022

Dosage forms

Dosage formProductsShare
System14100%

Marketing categories

Marketing categoryProductsShare
Authorized generics (NDA)1178.6%
New drug applications (NDA)321.4%

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.