Data / Drug companies / Antimycobacterial
Antimycobacterial drugs: 7 drugs from 27 companies in the FDA NDC directory
Antimycobacterial is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 48 products in this class from 27 companies, covering 7 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on December 23, 2025.
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.
- 27Companies
- 48Products
- 7Drugs by generic name
Drugs in the Antimycobacterial class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Isoniazid | 27 | 15 |
| Ethambutol hydrochloride | 13 | 7 |
| Pyrazinamide | 4 | 4 |
| Clofazimine | 1 | 1 |
| Pretomanid | 1 | 1 |
| Pyrazinamide tablet | 1 | 1 |
| Streptomycin | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Marlex Pharmaceuticals, Inc. | 5 | tablet; tablet, film coated | Generic drugs (ANDA) | March 1, 2025 |
| Remedyrepack Inc. | 4 | tablet | Generic drugs (ANDA) | December 23, 2025 |
| A-S Medication Solutions | 3 | tablet | Generic drugs (ANDA) | October 15, 2024 |
| Bryant Ranch Prepack | 3 | tablet | Generic drugs (ANDA) | November 1, 2024 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | October 15, 2024 |
| Chartwell RX, LLC | 2 | solution; tablet | Generic drugs (ANDA) | July 21, 1997 |
| Coupler LLC | 2 | tablet | Generic drugs (ANDA) | November 24, 2025 |
| Epic Pharma, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | March 18, 2015 |
| Genus Lifesciences | 2 | tablet | Generic drugs (ANDA) | November 1, 2024 |
| Kanchan Healthcare Inc | 2 | tablet, film coated | Authorized generics (NDA) | December 15, 2006 |
| Lupin Pharmaceuticals, Inc. | 2 | tablet | Generic drugs (ANDA) | July 10, 2009 |
| Omnivium Pharmaceuticals LLC. | 2 | tablet | Generic drugs (ANDA) | October 15, 2024 |
| Sti Pharma LLC | 2 | tablet, film coated | Authorized generics (NDA) | December 15, 2006 |
| Teva Pharmaceuticals USA, Inc. | 2 | tablet | Generic drugs (ANDA) | September 1, 1972 |
| American Health Packaging | 1 | tablet | Generic drugs (ANDA) | December 16, 2009 |
| American Health Packaging | 1 | tablet | Generic drugs (ANDA) | February 20, 2024 |
| Ani Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | May 11, 2021 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet | Generic drugs (ANDA) | September 1, 1972 |
| CMP Pharma, Inc. | 1 | solution | Generic drugs (ANDA) | November 11, 1983 |
| Hikma Pharmaceuticals USA Inc. | 1 | tablet | Generic drugs (ANDA) | August 30, 2024 |
| Macleods Pharmaceuticals Limited | 1 | tablet | Generic drugs (ANDA) | July 27, 2020 |
| Mylan Institutional Inc. | 1 | tablet | Generic drugs (ANDA) | June 9, 1994 |
| Novartis Pharmaceuticals Corporation | 1 | capsule, liquid filled | New drug applications (NDA) | December 15, 1986 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | September 1, 1972 |
| Sandoz Inc | 1 | injection, solution | Generic drugs (ANDA) | January 19, 2006 |
| Viatris Specialty LLC | 1 | tablet | New drug applications (NDA) | November 7, 2019 |
| XGen Pharmaceuticals DJB, Inc. | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | June 30, 1998 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 35 | 72.9% |
| Tablet, film coated | 8 | 16.7% |
| Solution | 2 | 4.2% |
| Injection, powder, lyophilized, for solution | 1 | 2.1% |
| Capsule, liquid filled | 1 | 2.1% |
| Injection, solution | 1 | 2.1% |
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.