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Data / Drug companies / Copper-containing Intrauterine Device

Copper-containing Intrauterine Device drugs: 13 drugs from 50 companies in the FDA NDC directory

Copper-containing Intrauterine Device is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 210 products in this class from 50 companies, covering 13 drugs by generic name. The main marketing category is unapproved homeopathic products, and the newest product started marketing on September 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.

  • 50Companies
  • 210Products
  • 13Drugs by generic name

Drugs in the Copper-containing Intrauterine Device class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Cuprum metallicum179
Copper164
Magnesium sulfate, copper sulfate21
Activated charcoal, copper, citrullus colocynthis fruit11
Agaricus muscarius, cuprum met, hypophysis, rhus tox11
Copper and arnica montana11
Cuprum 0.411
Cuprum 511
Cuprum met11
Cuprum metallicum 7x, 11x, 18x, 30x11
Renes cuprum11
Stannum complex 6x11
Zinc, copper, hypericum perforatum11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Deseret Biologicals, Inc.20liquidUnapproved homeopathic productsJanuary 5, 2026
BioActive Nutritional, Inc.18liquidUnapproved homeopathic productsJanuary 21, 2026
Energique, Inc.18liquidUnapproved homeopathic productsSeptember 30, 2026
Boiron16pellet; liquidUnapproved homeopathic productsOctober 2, 2023
Newton Laboratories, Inc.15liquid; pelletUnapproved homeopathic productsNovember 26, 2024
Professional Complementary Health Formulas11liquidUnapproved homeopathic productsAugust 15, 1984
Seroyal USA10liquidUnapproved homeopathic productsDecember 14, 2016
Hahnemann Laboratories, Inc.8pelletUnapproved homeopathic productsJune 16, 2022
Guna Spa7spray; solution/ dropsUnapproved homeopathic productsFebruary 17, 2021
Nutritional Specialties, Inc.7sprayUnapproved homeopathic productsMay 31, 2024
Uriel Pharmacy Inc.7ointment; liquidUnapproved homeopathic productsSeptember 1, 2009
Energetix Corporation6liquidUnapproved homeopathic productsNovember 3, 2017
Rubimed AG6liquidUnapproved homeopathic productsDecember 27, 2022
Ohm Pharma Inc.5liquid; pelletUnapproved homeopathic productsFebruary 10, 2020
Apex Energetics Inc.4solution/ dropsUnapproved homeopathic productsDecember 15, 1994
Natural Creations, Inc4liquid; syrupUnapproved homeopathic productsJune 1, 2016
True Botanica, LLC4liquid; globuleUnapproved homeopathic productsJuly 8, 2026
Dna Labs, Inc.3solutionUnapproved homeopathic productsJanuary 1, 1990
Homeocare Laboratories3pelletUnapproved homeopathic productsJuly 23, 2012
Homeolab International (Canada) Inc3liquid; tabletUnapproved homeopathic productsJanuary 1, 2020
CooperSurgical, Inc.2intrauterine deviceNew drug applications (NDA)August 15, 2024
DelCorean, LLC2lotionUnapproved homeopathic productsSeptember 1, 2008
Rxhomeo Private Limited D.B.A. Rxhomeo, Inc2pellet; liquidUnapproved homeopathic productsMay 23, 2024
Sevene USA2pelletUnapproved homeopathic productsJuly 8, 2022
Vitality Works, Inc.2liquidUnapproved homeopathic productsMarch 20, 2013
BM Private Limited1globuleUnapproved homeopathic productsJanuary 1, 2015
Bryant Ranch Prepack1tabletOther unapproved drugsOctober 1, 2018
Bryant Ranch Prepack1tabletOther unapproved drugsOctober 1, 2018
Exeltis USA, Inc.1capsule, gelatin coatedOther unapproved drugsJune 13, 2011
GMP Laboratories of America, Inc.1tabletUnapproved homeopathic productsJanuary 1, 2020
Guangzhou Renuma Medical Systems Co., Ltd1liquidUnapproved homeopathic productsOctober 26, 2017
Hyland's Inc.1tablet, solubleUnapproved homeopathic productsJanuary 1, 2010
InLight Creation, LLC.1sprayUnapproved homeopathic productsDecember 6, 2021
King Bio Inc.1liquidUnapproved homeopathic productsMarch 15, 2026
Liddell Laboratories, Inc.1sprayUnapproved homeopathic productsJuly 18, 2011
Marco Pharma International LLC.1liquidUnapproved homeopathic productsMarch 1, 1992
Method Pharmaceuticals, LLC1tabletOther unapproved drugsOctober 1, 2018
NaturalCare1tabletUnapproved homeopathic productsMarch 3, 2026
Nucleic Products, LLC1liquidUnapproved homeopathic productsMay 18, 2021
Organon LLC1intrauterine deviceNew drug applications (NDA)December 1, 2025
Quest Products, Inc.1ointmentUnapproved homeopathic productsJanuary 1, 2016
Remedyrepack Inc.1tabletOther unapproved drugsNovember 5, 2022
Silver Star Brands1liquidUnapproved homeopathic productsAugust 1, 2016
TRP Company1sprayUnapproved homeopathic productsAugust 6, 2024
The Magni Company1tabletUnapproved homeopathic productsSeptember 18, 2019
The Wellness Center for Research and Education, Inc.1liquidUnapproved homeopathic productsMarch 15, 2022
Total Operations Management LLC DBA:Bestmade Natural Products Micro1globuleUnapproved homeopathic productsJune 1, 2026
Walgreen Company1tabletUnapproved homeopathic productsMay 21, 2023
White Manufacturing Inc. DBA Micro-West1liquidUnapproved homeopathic productsJanuary 24, 2006
Zorex International1liquidUnapproved homeopathic productsDecember 22, 2021

Dosage forms

Dosage formProductsShare
Liquid12459%
Pellet3717.6%
Spray146.7%
Tablet104.8%
Solution/ drops62.9%
Globule31.4%
Solution31.4%
Ointment31.4%
Intrauterine device31.4%
Lotion21%
Gel10.5%
Capsule, gelatin coated10.5%

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.