Data / Drug companies / Platinum-based Drug
Platinum-based Drug drugs: 3 drugs from 24 companies in the FDA NDC directory
Platinum-based Drug is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 102 products in this class from 24 companies, covering 3 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 29, 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.
- 24Companies
- 102Products
- 3Drugs by generic name
Drugs in the Platinum-based Drug class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Oxaliplatin | 42 | 16 |
| Carboplatin | 40 | 11 |
| Cisplatin | 20 | 11 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Gland Pharma Limited | 11 | injection, solution; injection, powder, lyophilized, for solution | Generic drugs (ANDA) | November 6, 2017 |
| Teva Parenteral Medicines, Inc. | 10 | injection, solution | Generic drugs (ANDA) | January 19, 2016 |
| Eugia US LLC | 8 | injection, solution | Generic drugs (ANDA) | August 3, 2020 |
| Hospira, Inc. | 6 | injection, solution; injection, solution, concentrate | Generic drugs (ANDA) | May 23, 2022 |
| Meitheal Pharmaceuticals Inc. | 6 | injection, solution | Generic drugs (ANDA) | January 11, 2024 |
| Qilu Pharmaceutical Co., Ltd. | 5 | injection, solution; injection, powder, lyophilized, for solution | Generic drugs (ANDA) | June 7, 2016 |
| Apotex Corp. | 4 | injection, solution | Generic drugs (ANDA) | September 13, 2024 |
| BluePoint Laboratories | 4 | injection, solution; injection | Generic drugs (ANDA) | January 1, 2024 |
| Bpi Labs LLC | 4 | injection, solution | Generic drugs (ANDA) | July 31, 2023 |
| Fosun Pharma USA Inc. | 4 | injection, solution | Generic drugs (ANDA) | August 11, 2023 |
| Natco Pharma USA LLC | 4 | injection, solution | Generic drugs (ANDA) | July 2, 2026 |
| NorthStar RxLLC | 4 | injection, solution | Generic drugs (ANDA) | January 11, 2024 |
| Sandoz Inc | 4 | injection, solution | Generic drugs (ANDA) | July 1, 2016 |
| Teyro Labs Private Limited | 4 | injection, solution | Generic drugs (ANDA) | August 24, 2023 |
| WG Critical Care, LLC | 4 | injection, solution; injection, powder, lyophilized, for solution | New drug applications (NDA) | April 5, 2019 |
| Accord Healthcare Inc. | 3 | injection; injection, solution, concentrate | Generic drugs (ANDA) | May 17, 2018 |
| Avyxa Pharma, LLC | 3 | injection; injection, solution | New drug applications (NDA) | October 29, 2026 |
| Baxter Healthcare Corporation | 2 | injection, solution | Generic drugs (ANDA) | February 19, 2018 |
| Camber Pharmaceuticals, Inc. | 2 | injection, solution, concentrate | Generic drugs (ANDA) | January 27, 2025 |
| Fresenius Kabi USA, LLC | 2 | injection, solution | Generic drugs (ANDA) | December 11, 2009 |
| Hikma Pharmaceuticals USA Inc. | 2 | injection | Generic drugs (ANDA) | November 7, 2000 |
| Mylan Institutional LLC | 2 | injection, solution | Generic drugs (ANDA) | August 25, 2014 |
| Sagent Pharmaceuticals | 2 | injection, solution | Generic drugs (ANDA) | July 1, 2023 |
| Shandong New Time Pharmaceutical Co., Ltd. | 2 | injection, solution | Generic drugs (ANDA) | January 15, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 86 | 84.3% |
| Injection | 7 | 6.9% |
| Injection, powder, lyophilized, for solution | 5 | 4.9% |
| Injection, solution, concentrate | 4 | 3.9% |
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.