Data / Drug companies / Nitrogen Binding Agent
Nitrogen Binding Agent drugs: 10 drugs from 43 companies in the FDA NDC directory
Nitrogen Binding Agent is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 117 products in this class from 43 companies, covering 10 drugs by generic name. The main marketing category is unapproved homeopathic products, and the newest product started marketing on October 12, 2026.
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- 43Companies
- 117Products
- 10Drugs by generic name
Drugs in the Nitrogen Binding Agent class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Glycerol phenylbutyrate | 8 | 8 |
| Sodium phenylacetate and sodium benzoate | 10 | 7 |
| Sodium phenylbutyrate | 7 | 7 |
| Glycerol phenylbutyrate oral | 2 | 2 |
| Acidum benzoicum | 8 | 1 |
| Benzoic acid | 3 | 1 |
| Benzoic acid, salicylic acid, sulfur | 1 | 1 |
| Benzoicum acidum | 1 | 1 |
| Dmae | 1 | 1 |
| Sodium phenylbutyrate tablets, 500 mg | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Newton Laboratories, Inc. | 22 | liquid; pellet | Unapproved homeopathic products | September 19, 2025 |
| Deseret Biologicals, Inc. | 12 | liquid | Unapproved homeopathic products | June 15, 2026 |
| Hahnemann Laboratories, Inc. | 8 | pellet | Unapproved homeopathic products | April 14, 2022 |
| Professional Complementary Health Formulas | 6 | liquid | Unapproved homeopathic products | August 15, 1984 |
| Anubis Cosmetics SL | 5 | concentrate; lotion | Over the counter monograph drugs | January 13, 2023 |
| BioActive Nutritional, Inc. | 5 | liquid | Unapproved homeopathic products | January 7, 2025 |
| Boiron | 4 | pellet; tablet | Unapproved homeopathic products | January 1, 2024 |
| Navinta LLC | 4 | injection, solution, concentrate; tablet | Generic drugs (ANDA) | July 11, 2026 |
| Energetix Corporation | 3 | liquid | Unapproved homeopathic products | April 1, 2017 |
| Horizon Therapeutics USA, Inc. | 3 | liquid; tablet | New drug applications (NDA) | February 28, 2013 |
| Par Health USA, LLC | 3 | powder; liquid | Generic drugs (ANDA) | October 17, 2025 |
| Pekana Naturheilmittel GmbH | 3 | solution/ drops; liquid | Unapproved homeopathic products | June 24, 2019 |
| Zydus Pharmaceuticals USA Inc. | 3 | liquid; injection, solution, concentrate | Generic drugs (ANDA) | May 4, 2026 |
| Energique, Inc. | 2 | liquid | Unapproved homeopathic products | June 25, 2026 |
| Maia Pharmaceuticals, Inc. | 2 | injection, solution, concentrate; injection | Generic drugs (ANDA) | July 1, 2021 |
| Nutritional Specialties, Inc. | 2 | spray | Unapproved homeopathic products | October 4, 2023 |
| Ohm Pharma Inc. | 2 | liquid; pellet | Unapproved homeopathic products | November 1, 2019 |
| Omnivium Pharmaceuticals LLC. | 2 | injection, solution, concentrate | Generic drugs (ANDA) | May 15, 2025 |
| Silver Star Brands | 2 | tablet; liquid | Unapproved homeopathic products | April 3, 2023 |
| Ailex Pharmaceuticals, LLC | 1 | injection, solution, concentrate | Generic drugs (ANDA) | February 24, 2016 |
| Apex Energetics Inc. | 1 | solution/ drops | Unapproved homeopathic products | August 15, 1988 |
| Aurobindo Pharma Limited | 1 | liquid | Generic drugs (ANDA) | April 15, 2026 |
| BM Private Limited | 1 | liquid | Unapproved homeopathic products | January 1, 2015 |
| Camber Pharmaceuticals, Inc. | 1 | liquid | Generic drugs (ANDA) | August 21, 2026 |
| Cintex Services, LLC | 1 | tablet | Other unapproved drugs | October 5, 2026 |
| Fosun Pharma USA Inc. | 1 | injection | New drug applications (NDA) | November 14, 2021 |
| GMP Laboratories of America, Inc. | 1 | tablet | Unapproved homeopathic products | January 1, 2020 |
| Glenmark Pharmaceuticals Inc., USA | 1 | tablet | Generic drugs (ANDA) | November 1, 2022 |
| Health Masters LLC | 1 | liquid | Unapproved homeopathic products | February 27, 2020 |
| Homeolab International (Canada) Inc | 1 | tablet | Unapproved homeopathic products | January 1, 2020 |
| Laboratorios H.G. C.A. | 1 | cream | Over the counter monograph drugs | April 22, 2024 |
| Lupin Pharmaceuticals, Inc. | 1 | liquid | New drug applications (NDA) | October 20, 2025 |
| Medunik | 1 | pellet | New drug applications (NDA) | September 14, 2022 |
| Mission Pharmacal Company | 1 | tablet, coated | Other unapproved drugs | November 7, 2023 |
| Novadoz Pharmaceuticals LLC | 1 | liquid | Generic drugs (ANDA) | April 15, 2026 |
| Pai Holdings, LLC DBA Pai Pharma | 1 | liquid | Generic drugs (ANDA) | October 12, 2026 |
| Seroyal USA | 1 | liquid | Unapproved homeopathic products | December 14, 2015 |
| Supplement Clinic, LLC. | 1 | liquid | Unapproved homeopathic products | November 1, 2017 |
| Teva Pharmaceuticals, Inc. | 1 | liquid | Generic drugs (ANDA) | April 16, 2026 |
| Total Operations Management LLC DBA:Bestmade Natural Products Micro | 1 | liquid | Unapproved homeopathic products | January 1, 2015 |
| VitaminMed, LLC | 1 | spray | Unapproved homeopathic products | December 8, 2016 |
| Xymogen | 1 | liquid | Unapproved homeopathic products | May 8, 2020 |
| Zydus Pharmaceuticals USA Inc. | 1 | injection, solution, concentrate | Generic drugs (ANDA) | February 8, 2021 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Liquid | 61 | 52.1% |
| Pellet | 21 | 17.9% |
| Tablet | 10 | 8.5% |
| Injection, solution, concentrate | 8 | 6.8% |
| Solution/ drops | 3 | 2.6% |
| Concentrate | 3 | 2.6% |
| Spray | 3 | 2.6% |
| Injection | 2 | 1.7% |
| Powder | 2 | 1.7% |
| Lotion | 2 | 1.7% |
| Cream | 1 | 0.9% |
| Tablet, coated | 1 | 0.9% |
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.