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Data / Drug companies / Clonidine

Clonidine: 9 companies and 16 products in the FDA NDC directory

Clonidine is listed in the FDA National Drug Code Directory by 9 companies, with 16 products in commercial distribution. 13 of the products (81.2%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are patch; patch, extended release; tablet, extended release, and the newest product started marketing on February 10, 2024.

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Companies listing it
9
Products
16
Generic (ANDA) products
13 (81.2%)
Application numbers
6
Routes
Transdermal, Oral, Epidural
Brand names
Nexiclon XR
openFDA record search
api.fda.gov

Companies that list clonidine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Actavis Pharma, Inc.3patchGeneric drugs (ANDA)May 6, 2014
Dr. Reddy's Laboratories Inc.3patch, extended releaseGeneric drugs (ANDA)February 10, 2024
Mylan Pharmaceuticals Inc.3patchGeneric drugs (ANDA)March 4, 2013
XGen Pharmaceuticals DJB, Inc.2injection, solutionGeneric drugs (ANDA)October 29, 2013
Ingenus Pharmaceuticals, LLC1tablet, extended releaseGeneric drugs (ANDA)March 5, 2019
Mayne Pharma Inc.1patch, extended releaseGeneric drugs (ANDA)August 3, 2016
Palmetto Pharmaceuticals Inc.1tablet, extended releaseAuthorized generics (NDA)March 1, 2022
Rosemont Pharmaceuticals LLC1tablet, extended releaseNew drug applications (NDA)March 1, 2022
TruPharma, LLC1tablet, extended releaseAuthorized generics (NDA)January 11, 2024

Dosage forms

Dosage formProductsShare
Patch637.5%
Patch, extended release425%
Tablet, extended release425%
Injection, solution212.5%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1381.2%
Authorized generics (NDA)212.5%
New drug applications (NDA)16.2%

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.