Data / Drug companies / Methylprednisolone
Methylprednisolone: 31 companies and 60 products in the FDA NDC directory
Methylprednisolone is listed in the FDA National Drug Code Directory by 31 companies, with 60 products in commercial distribution. 50 of the products (83.3%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; injection, powder, lyophilized, for solution, and the newest product started marketing on May 1, 2025.
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- Companies listing it
- 31
- Products
- 60
- Generic (ANDA) products
- 50 (83.3%)
- Application numbers
- 8
- Routes
- Oral, Intramuscular, Intravenous
- Brand names
- Medrol
- openFDA record search
- api.fda.gov
Companies that list methylprednisolone
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Chartwell RX, LLC | 5 | tablet | Generic drugs (ANDA) | February 22, 2019 |
| Tianjin Kingyork Pharmaceuticals Co., Ltd | 5 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | April 20, 2021 |
| Mylan Pharmaceuticals Inc. | 4 | tablet | Authorized generics (NDA) | March 25, 2013 |
| Pharmacia & Upjohn Company LLC | 4 | tablet | New drug applications (NDA) | September 20, 2013 |
| Zydus Lifesciences Limited | 4 | tablet | Generic drugs (ANDA) | May 1, 2018 |
| Zydus Pharmaceuticals USA Inc. | 4 | tablet | Generic drugs (ANDA) | May 1, 2018 |
| Advanced Rx of Tennessee, LLC | 3 | tablet | Generic drugs (ANDA) | January 11, 2023 |
| Remedyrepack Inc. | 3 | tablet | Generic drugs (ANDA) | October 14, 2024 |
| A-S Medication Solutions | 2 | tablet | Generic drugs (ANDA) | May 1, 2018 |
| Amneal Pharmaceuticals LLC | 2 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | November 11, 2016 |
| Asclemed USA, Inc. | 2 | tablet | Generic drugs (ANDA) | May 14, 2018 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | December 22, 1998 |
| NuCare Pharmaceuticals,Inc. | 2 | tablet | Authorized generics (NDA) | May 14, 2018 |
| American Health Packaging | 1 | tablet | Generic drugs (ANDA) | December 3, 2013 |
| BluePoint Laboratories | 1 | tablet | Generic drugs (ANDA) | May 1, 2025 |
| Bryant Ranch Prepack | 1 | tablet | Generic drugs (ANDA) | December 22, 1998 |
| Direct_Rx | 1 | tablet | Generic drugs (ANDA) | September 13, 2021 |
| Doc Rx | 1 | tablet | Generic drugs (ANDA) | May 14, 2018 |
| Epic Pharma, LLC | 1 | tablet | Generic drugs (ANDA) | May 14, 2018 |
| Hawaii Repack, Inc. | 1 | tablet | Generic drugs (ANDA) | May 14, 2018 |
| Major Pharmaceuticals | 1 | tablet | Generic drugs (ANDA) | May 1, 2018 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | December 22, 1998 |
| Par Health USA, LLC | 1 | tablet | Generic drugs (ANDA) | December 22, 1998 |
| Phoenix RX LLC | 1 | tablet | Generic drugs (ANDA) | May 14, 2018 |
| Preferred Pharmaceuticals Inc. | 1 | tablet | Generic drugs (ANDA) | January 5, 2021 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | May 14, 2018 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | October 31, 1997 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | May 1, 2018 |
| Sportpharm LLC | 1 | tablet | Generic drugs (ANDA) | May 14, 2018 |
| St. Mary's Medical Park Pharmacy | 1 | tablet | Generic drugs (ANDA) | September 6, 2024 |
| Tianjin Tianyao Pharmaceuticals Co., Ltd. | 1 | tablet | Generic drugs (ANDA) | May 14, 2018 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 53 | 88.3% |
| Injection, powder, lyophilized, for solution | 7 | 11.7% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 50 | 83.3% |
| Authorized generics (NDA) | 6 | 10% |
| New drug applications (NDA) | 4 | 6.7% |
Pharmacologic classes
| Class | Products |
|---|---|
| Corticosteroid | 60 |
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.