Data / Drug companies / Janssen Products, LP
Janssen Products, LP: 29 products in the FDA NDC directory, labeler code 59676
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Janssen Products, LP (labeler code 59676) lists 29 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 29 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on February 27, 2026.
The request: Watch Janssen Products, LP (FDA labeler code 59676): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 59676
- Products in commercial distribution
- 29
- Packages
- 35
- Finished drugs by generic name
- 9
- Prescription products
- 29
- Over the counter products
- 0
- Flagged as original packager
- 29 of 29 products that carry the flag
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- June 1, 1989
- 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) | 22 | 75.9% |
| Biologics (BLA) | 7 | 24.1% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 29 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Erythropoietin | 7 | 1 |
| Darunavir | 5 | 14 |
| Darunavir ethanolate and cobicistat | 3 | 2 |
| Etravirine | 3 | 7 |
| Erdafitinib | 3 | 1 |
| Rilpivirine hydrochloride | 2 | 1 |
| Apalutamide | 2 | 1 |
| Bedaquiline fumarate | 2 | 1 |
| Trabectedin | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 13 | 44.8% |
| Injection, solution | 7 | 24.1% |
| Tablet | 5 | 17.2% |
| Tablet, for suspension | 2 | 6.9% |
| Injection, powder, lyophilized, for solution | 1 | 3.4% |
| Suspension | 1 | 3.4% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Prezcobix ped | 59676-577 | Tablet, for suspension | New drug applications (NDA) | February 27, 2026 |
| Prezcobix | 59676-578 | Tablet, film coated | New drug applications (NDA) | March 21, 2025 |
| Edurant ped | 59676-280 | Tablet, for suspension | New drug applications (NDA) | March 15, 2024 |
| Sirturo | 59676-702 | Tablet | New drug applications (NDA) | May 27, 2020 |
| Balversa | 59676-050 | Tablet, film coated | New drug applications (NDA) | April 12, 2019 |
| Balversa | 59676-040 | Tablet, film coated | New drug applications (NDA) | April 12, 2019 |
| Balversa | 59676-030 | Tablet, film coated | New drug applications (NDA) | April 12, 2019 |
| Symtuza | 59676-800 | Tablet, film coated | New drug applications (NDA) | July 17, 2018 |
| Erleada | 59676-604 | Tablet, film coated | New drug applications (NDA) | February 14, 2018 |
| Erleada | 59676-600 | Tablet, film coated | New drug applications (NDA) | February 14, 2018 |
| Yondelis | 59676-610 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | October 23, 2015 |
| Prezcobix | 59676-575 | Tablet, film coated | New drug applications (NDA) | January 31, 2015 |
| Sirturo | 59676-701 | Tablet | New drug applications (NDA) | December 28, 2012 |
| Prezista | 59676-566 | Tablet, film coated | New drug applications (NDA) | November 9, 2012 |
| Intelence | 59676-572 | Tablet | New drug applications (NDA) | March 26, 2012 |
| Prezista | 59676-565 | Suspension | New drug applications (NDA) | December 16, 2011 |
| Edurant | 59676-278 | Tablet, film coated | New drug applications (NDA) | May 20, 2011 |
| Intelence | 59676-571 | Tablet | New drug applications (NDA) | December 22, 2010 |
| Prezista | 59676-564 | Tablet, film coated | New drug applications (NDA) | April 27, 2009 |
| Prezista | 59676-563 | Tablet, film coated | New drug applications (NDA) | January 14, 2009 |
| Prezista | 59676-562 | Tablet, film coated | New drug applications (NDA) | March 8, 2008 |
| Intelence | 59676-570 | Tablet | New drug applications (NDA) | January 18, 2008 |
| Procrit | 59676-340 | Injection, solution | Biologics (BLA) | June 1, 1989 |
| Procrit | 59676-320 | Injection, solution | Biologics (BLA) | June 1, 1989 |
| Procrit | 59676-312 | Injection, solution | Biologics (BLA) | June 1, 1989 |
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.