Data / Drug companies / Medexus Pharma, Inc.
Medexus Pharma, Inc.: 18 products in the FDA NDC directory, labeler code 59137
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Medexus Pharma, Inc. (labeler code 59137) lists 18 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 18 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on January 28, 2025.
The request: Watch Medexus Pharma, Inc. (FDA labeler code 59137): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 59137
- Products in commercial distribution
- 18
- Packages
- 25
- Finished drugs by generic name
- 4
- Prescription products
- 18
- Over the counter products
- 0
- Flagged as original packager
- 17 of 17 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- July 10, 2014
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 11 | 61.1% |
| Biologics (BLA) | 6 | 33.3% |
| Unapproved drugs for a shortage | 1 | 5.6% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 18 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Methotrexate | 9 | 31 |
| Coagulation factor ix (recombinant) | 6 | 3 |
| Treosulfan | 2 | 1 |
| Triamcinolone hexacetonide | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 9 | 50% |
| Kit | 6 | 33.3% |
| Injection, powder, lyophilized, for solution | 2 | 11.1% |
| Injection, suspension | 1 | 5.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Folate Analog Metabolic Inhibitor | 9 |
| Corticosteroid | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Grafapex | 59137-365 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | January 28, 2025 |
| Grafapex | 59137-335 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | January 28, 2025 |
| Hexatrione 2% | 59137-570 | Injection, suspension | Unapproved drugs for a shortage | March 3, 2021 |
| Ixinity | 59137-289 | Kit | Biologics (BLA) | May 12, 2017 |
| Ixinity | 59137-288 | Kit | Biologics (BLA) | May 12, 2017 |
| Ixinity | 59137-287 | Kit | Biologics (BLA) | May 12, 2017 |
| Ixinity | 59137-284 | Kit | Biologics (BLA) | May 12, 2017 |
| Ixinity | 59137-283 | Kit | Biologics (BLA) | May 12, 2017 |
| Ixinity | 59137-282 | Kit | Biologics (BLA) | May 12, 2017 |
| Rasuvo | 59137-550 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
| Rasuvo | 59137-540 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
| Rasuvo | 59137-535 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
| Rasuvo | 59137-530 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
| Rasuvo | 59137-525 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
| Rasuvo | 59137-520 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
| Rasuvo | 59137-515 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
| Rasuvo | 59137-510 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
| Rasuvo | 59137-505 | Injection, solution | New drug applications (NDA) | July 10, 2014 |
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.