Data / Drug companies / Carnitine Analog
Carnitine Analog drugs: 2 drugs from 18 companies in the FDA NDC directory
Carnitine Analog is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 29 products in this class from 18 companies, covering 2 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on September 30, 2026.
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- 18Companies
- 29Products
- 2Drugs by generic name
Drugs in the Carnitine Analog class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Levocarnitine | 16 | 10 |
| Levocarnitine oral | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Leadiant Biosciences, Inc. | 4 | solution; injection, solution | New drug applications (NDA) | December 16, 1992 |
| Ani Pharmaceuticals, Inc. | 3 | solution; tablet | Generic drugs (ANDA) | December 9, 2022 |
| Energique, Inc. | 3 | liquid | Unapproved homeopathic products | January 28, 2025 |
| Professional Complementary Health Formulas | 3 | liquid | Unapproved homeopathic products | August 15, 1984 |
| American Regent, Inc. | 2 | injection, solution | Generic drugs (ANDA) | June 21, 2023 |
| BioActive Nutritional, Inc. | 2 | liquid | Unapproved homeopathic products | January 3, 2025 |
| Baxter Healthcare Corporation | 1 | injection, solution | Generic drugs (ANDA) | July 2, 2026 |
| Deseret Biologicals, Inc. | 1 | liquid | Unapproved homeopathic products | October 10, 2023 |
| Devatis, Inc. | 1 | injection, solution | Generic drugs (ANDA) | November 1, 2025 |
| Gland Pharma Limited | 1 | injection, solution | Generic drugs (ANDA) | September 30, 2026 |
| Guna Spa | 1 | solution/ drops | Unapproved homeopathic products | May 27, 2010 |
| Hikma Pharmaceuticals USA Inc. | 1 | injection | Generic drugs (ANDA) | June 1, 2023 |
| Liddell Laboratories, Inc. | 1 | spray | Unapproved homeopathic products | July 26, 2021 |
| Nutritional Specialties, Inc. | 1 | spray | Unapproved homeopathic products | July 7, 2023 |
| Rising Pharma Holdings, Inc. | 1 | tablet | Generic drugs (ANDA) | December 1, 2020 |
| Rising Pharma Holdings, Inc. | 1 | solution | Generic drugs (ANDA) | September 20, 2004 |
| Saptalis Pharmaceuticals, LLC. | 1 | solution | Generic drugs (ANDA) | February 21, 2024 |
| TruPharma, LLC | 1 | solution | Generic drugs (ANDA) | February 9, 2022 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Liquid | 9 | 31% |
| Solution | 7 | 24.1% |
| Injection, solution | 6 | 20.7% |
| Tablet | 3 | 10.3% |
| Spray | 2 | 6.9% |
| Solution/ drops | 1 | 3.4% |
| Injection | 1 | 3.4% |
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.