Data / Drug companies / Parenteral Iron Replacement
Parenteral Iron Replacement drugs: 14 drugs from 37 companies in the FDA NDC directory
Parenteral Iron Replacement is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 81 products in this class from 37 companies, covering 14 drugs by generic name. The main marketing category is unapproved homeopathic products, and the newest product started marketing on August 31, 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.
- 37Companies
- 81Products
- 14Drugs by generic name
Drugs in the Parenteral Iron Replacement class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Iron sucrose | 15 | 5 |
| Ferric carboxymaltose | 4 | 3 |
| Ferumoxytol | 4 | 3 |
| Ferric citrate | 3 | 3 |
| Iron dextran | 3 | 3 |
| Ferrum muriaticum | 8 | 2 |
| Ferric carboxymaltose injection | 3 | 2 |
| Ferric picrate | 3 | 1 |
| Ferric subsulfate | 2 | 1 |
| Sodium ferric gluconate complex | 2 | 1 |
| Sodium ferric gluconate complex in sucrose | 2 | 1 |
| Ferric maltol | 1 | 1 |
| Ferric sulfate | 1 | 1 |
| Venofer (iron sucrose) | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| American Regent, Inc. | 7 | injection, solution | New drug applications (NDA) | June 1, 2022 |
| Hahnemann Laboratories, Inc. | 7 | pellet | Unapproved homeopathic products | July 6, 2022 |
| Kadesh Incoporation Co,Ltd | 5 | liquid; spray | Unapproved homeopathic products | August 18, 2023 |
| Sandoz Inc | 5 | injection; injection, solution | Generic drugs (ANDA) | July 3, 2026 |
| Mylan Institutional LLC | 4 | injection, solution | Generic drugs (ANDA) | July 1, 2026 |
| Professional Complementary Health Formulas | 4 | liquid | Unapproved homeopathic products | August 15, 1984 |
| Boiron | 3 | pellet | Unapproved homeopathic products | January 1, 2025 |
| Dna Labs, Inc. | 3 | solution; solution/ drops | Unapproved homeopathic products | January 1, 1990 |
| Guna Spa | 3 | solution/ drops | Unapproved homeopathic products | September 24, 2020 |
| International Medication Systems, Limited | 3 | injection | Generic drugs (ANDA) | September 12, 2025 |
| Azurity Pharmaceuticals, Inc. | 2 | injection | New drug applications (NDA) | October 20, 2025 |
| Deseret Biologicals, Inc. | 2 | liquid | Unapproved homeopathic products | October 10, 2023 |
| Fresenius Medical Care Renal Therapies Group, LLC | 2 | injection, solution | New drug applications (NDA) | January 27, 2011 |
| HF Acquisition Co LLC, DBA HealthFirst | 2 | injection; injection, solution | New drug applications (NDA) | June 25, 2021 |
| Hikma Pharmaceuticals USA Inc. | 2 | injection | Generic drugs (ANDA) | March 31, 2011 |
| Mylan Institutional LLC | 2 | injection, solution | Generic drugs (ANDA) | August 31, 2026 |
| Newton Laboratories, Inc. | 2 | liquid | Unapproved homeopathic products | September 2, 2019 |
| Premier Dental Products Company | 2 | paste | Other unapproved drugs | November 29, 2024 |
| Sanofi-Aventis U.S. LLC | 2 | injection | New drug applications (NDA) | July 7, 2014 |
| Vitality Works, Inc. | 2 | liquid | Unapproved homeopathic products | April 4, 2013 |
| Akebia Therapeutics, Inc. | 1 | tablet, film coated | New drug applications (NDA) | September 17, 2014 |
| Allergan, Inc. | 1 | injection | New drug applications (NDA) | April 29, 1974 |
| Amag Pharmaceuticals, Inc | 1 | injection | New drug applications (NDA) | July 13, 2009 |
| BM Private Limited | 1 | liquid | Unapproved homeopathic products | January 1, 2015 |
| BioActive Nutritional, Inc. | 1 | liquid | Unapproved homeopathic products | January 21, 2013 |
| Gingi-Pak a Division of the Belport | 1 | solution | Other unapproved drugs | June 26, 1987 |
| Henry Schein, Inc. | 1 | injection | New drug applications (NDA) | January 11, 2022 |
| JoyWell Co LLC | 1 | pellet | Unapproved homeopathic products | November 19, 2025 |
| Mylan Pharmaceuticals Inc. | 1 | tablet, film coated | Authorized generics (NDA) | March 20, 2025 |
| Nutritional Specialties, Inc. | 1 | liquid | Unapproved homeopathic products | March 29, 2023 |
| PureTek Corporation | 1 | capsule | Other unapproved drugs | June 1, 2011 |
| Seton Pharmaceuticals | 1 | capsule, gelatin coated | Other unapproved drugs | October 1, 2009 |
| Shield TX (uk) Ltd | 1 | capsule | New drug applications (NDA) | July 1, 2021 |
| Teva Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 11, 2026 |
| Total Operations Management LLC DBA:Bestmade Natural Products Micro | 1 | liquid | Unapproved homeopathic products | January 1, 2015 |
| True Botanica, LLC | 1 | globule | Unapproved homeopathic products | February 3, 2014 |
| Uriel Pharmacy Inc. | 1 | liquid | Unapproved homeopathic products | September 1, 2009 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 17 | 21% |
| Liquid | 17 | 21% |
| Injection, solution | 17 | 21% |
| Pellet | 11 | 13.6% |
| Solution/ drops | 4 | 4.9% |
| Solution | 3 | 3.7% |
| Tablet, film coated | 3 | 3.7% |
| Capsule | 2 | 2.5% |
| Spray | 2 | 2.5% |
| Paste | 2 | 2.5% |
| Capsule, gelatin coated | 1 | 1.2% |
| Globule | 1 | 1.2% |
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.