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Data / Drug companies / Clonidine transdermal system

Clonidine transdermal system: 2 companies and 12 products in the FDA NDC directory

Clonidine transdermal system is listed in the FDA National Drug Code Directory by 2 companies, with 12 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 patch, and the newest product started marketing on March 30, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
2
Products
12
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Transdermal
Brand names
Catapres-TTS-3, Catapres-TTS-1, Catapres-TTS-2
openFDA record search
api.fda.gov

Companies that list clonidine transdermal system

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Technomed Inc.6patchNew drug applications (NDA)March 30, 2026
TruPharma, LLC6patchAuthorized generics (NDA)March 30, 2026

Dosage forms

Dosage formProductsShare
Patch12100%

Marketing categories

Marketing categoryProductsShare
Authorized generics (NDA)650%
New drug applications (NDA)650%

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.