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Data / Drug companies / Copper Chelator

Copper Chelator drugs: 2 drugs from 5 companies in the FDA NDC directory

Copper Chelator is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 6 products in this class from 5 companies, covering 2 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on September 22, 2023.

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.

  • 5Companies
  • 6Products
  • 2Drugs by generic name

Drugs in the Copper Chelator class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Trientine hydrochloride57
Trientine tetrahydrochloride11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Rising Pharma Holdings, Inc.2capsuleGeneric drugs (ANDA)September 22, 2023
Dr. Reddy's Laboratories Inc.1capsuleGeneric drugs (ANDA)July 3, 2019
Navinta LLC1capsuleGeneric drugs (ANDA)December 5, 2020
Orphalan SA1tablet, film coatedNew drug applications (NDA)September 14, 2022
Par Health USA, LLC1capsuleGeneric drugs (ANDA)September 27, 2019

Dosage forms

Dosage formProductsShare
Capsule583.3%
Tablet, film coated116.7%

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.