Data / Drug companies / Paramagnetic Contrast Agent
Paramagnetic Contrast Agent drugs: 15 drugs from 26 companies in the FDA NDC directory
Paramagnetic Contrast Agent is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 160 products in this class from 26 companies, covering 15 drugs by generic name. The main marketing category is unapproved homeopathic products, and the newest product started marketing on August 21, 2026.
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- 26Companies
- 160Products
- 15Drugs by generic name
Drugs in the Paramagnetic Contrast Agent class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Folic acid | 7 | 34 |
| Gadoteridol | 3 | 2 |
| Manganese | 1 | 2 |
| Manganum fluoratum | 16 | 1 |
| Manganum bromatum | 8 | 1 |
| Manganum carbonicum | 8 | 1 |
| Manganum iodatum | 8 | 1 |
| Manganum muriaticum | 8 | 1 |
| Manganum phosphoricum | 8 | 1 |
| Manganum sulphuricum | 7 | 1 |
| Manganese acetate tetrahydrate | 4 | 1 |
| Trace elements injection 4 | 2 | 1 |
| Gadodiamide | 1 | 1 |
| Manganese chloride | 1 | 1 |
| Trace elements 4 | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Hahnemann Laboratories, Inc. | 63 | pellet | Unapproved homeopathic products | March 27, 2023 |
| PureTek Corporation | 27 | tablet; capsule | Other unapproved drugs | August 21, 2026 |
| Deseret Biologicals, Inc. | 15 | liquid | Unapproved homeopathic products | June 2, 2026 |
| BioActive Nutritional, Inc. | 14 | liquid | Unapproved homeopathic products | February 13, 2024 |
| Energique, Inc. | 7 | liquid | Unapproved homeopathic products | February 18, 2026 |
| Guna Spa | 5 | solution/ drops; pellet | Unapproved homeopathic products | May 27, 2010 |
| American Regent, Inc. | 4 | injection, solution; injection, solution, concentrate | Other unapproved drugs | September 1, 2021 |
| Boiron | 4 | pellet | Unapproved homeopathic products | January 1, 2024 |
| Bracco Diagnostics Inc | 2 | injection, solution | New drug applications (NDA) | October 9, 2003 |
| Energetix Corporation | 2 | liquid | Unapproved homeopathic products | October 22, 2014 |
| Vitality Works, Inc. | 2 | liquid | Unapproved homeopathic products | April 8, 2013 |
| Attuned Matrix, LLC | 1 | spray | Unapproved homeopathic products | May 2, 2023 |
| Carnivora Research International | 1 | liquid | Unapproved homeopathic products | September 6, 2022 |
| Fresenius Kabi USA, LLC | 1 | injection, solution | Generic drugs (ANDA) | November 17, 2025 |
| GE Healthcare Inc. | 1 | injection | New drug applications (NDA) | April 19, 2002 |
| Hospira, Inc. | 1 | injection, solution | New drug applications (NDA) | January 31, 2005 |
| King Bio Inc. | 1 | liquid | Unapproved homeopathic products | March 15, 2026 |
| Newton Laboratories, Inc. | 1 | liquid | Unapproved homeopathic products | January 1, 2019 |
| Nucleic Products, LLC | 1 | liquid | Unapproved homeopathic products | May 18, 2021 |
| Nutritional Specialties, Inc. | 1 | spray | Unapproved homeopathic products | March 31, 2023 |
| Ohm Pharma Inc. | 1 | spray | Unapproved homeopathic products | December 19, 2018 |
| Pekana Naturheilmittel GmbH | 1 | solution/ drops | Unapproved homeopathic products | June 24, 2019 |
| Professional Complementary Health Formulas | 1 | liquid | Unapproved homeopathic products | August 15, 1984 |
| Seton Pharmaceuticals | 1 | capsule, gelatin coated | Other unapproved drugs | October 1, 2009 |
| Slate Run Pharmaceuticals, LLC | 1 | injection | Generic drugs (ANDA) | February 20, 2025 |
| U.S. Pharmaceutical Corporation | 1 | capsule | Other unapproved drugs | January 1, 2009 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Pellet | 68 | 42.5% |
| Liquid | 45 | 28.1% |
| Tablet | 25 | 15.6% |
| Injection, solution | 7 | 4.4% |
| Solution/ drops | 4 | 2.5% |
| Spray | 4 | 2.5% |
| Capsule | 3 | 1.9% |
| Injection | 2 | 1.2% |
| Injection, solution, concentrate | 1 | 0.6% |
| Capsule, gelatin coated | 1 | 0.6% |
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.