Data / Drug companies / Novartis Pharma Stein AG
Novartis Pharma Stein AG: 39 products in the FDA NDC directory, labeler code 17088
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Novartis Pharma Stein AG (labeler code 17088) lists 39 products in the FDA National Drug Code Directory. By type: 39 prescription drugs. Its main marketing category is drugs for further processing. The newest product started marketing on March 14, 2024.
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- Labeler code
- 17088
- Products in commercial distribution
- 39
- Packages
- 39
- Finished drugs by generic name
- 0
- Prescription products
- 39
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- November 14, 1983
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Drugs for further processing | 39 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 39 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 14 | 35.9% |
| Tablet, film coated | 9 | 23.1% |
| Injection, solution | 5 | 12.8% |
| Capsule | 4 | 10.3% |
| Tablet, for suspension | 4 | 10.3% |
| Injection | 1 | 2.6% |
| Injection, solution, concentrate | 1 | 2.6% |
| Injection, powder, for solution | 1 | 2.6% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Tislelizumab-jsgr | 17088-0378 | Injection, solution, concentrate | Drugs for further processing | March 14, 2024 |
| Omalizumab | 17088-0282 | Injection, solution | Drugs for further processing | August 18, 2023 |
| Dabrafenib | 17088-0212 | Tablet, for suspension | Drugs for further processing | March 16, 2023 |
| Alpelisib | 17088-0346 | Tablet | Drugs for further processing | April 5, 2022 |
| Alpelisib | 17088-0205 | Tablet | Drugs for further processing | April 5, 2022 |
| Alpelisib | 17088-0198 | Tablet | Drugs for further processing | April 5, 2022 |
| Asciminib | 17088-0330 | Tablet, film coated | Drugs for further processing | October 29, 2021 |
| Asciminib | 17088-0163 | Tablet, film coated | Drugs for further processing | October 29, 2021 |
| Asciminib | 17088-0156 | Tablet, film coated | Drugs for further processing | October 29, 2021 |
| Alpelisib | 17088-0322 | Tablet | Drugs for further processing | May 24, 2019 |
| Alpelisib | 17088-0254 | Tablet | Drugs for further processing | May 24, 2019 |
| Alpelisib | 17088-0170 | Tablet | Drugs for further processing | May 24, 2019 |
| Siponimod | 17088-0191 | Tablet, film coated | Drugs for further processing | March 26, 2019 |
| Siponimod | 17088-0184 | Tablet, film coated | Drugs for further processing | March 26, 2019 |
| Siponimod | 17088-0177 | Tablet, film coated | Drugs for further processing | March 26, 2019 |
| Omalizumab | 17088-0275 | Injection, solution | Drugs for further processing | September 28, 2018 |
| Omalizumab | 17088-0268 | Injection, solution | Drugs for further processing | September 28, 2018 |
| Canakinumab | 17088-0354 | Injection, solution | Drugs for further processing | December 22, 2016 |
| Trametinib | 17088-0128 | Tablet, film coated | Drugs for further processing | March 17, 2016 |
| Trametinib | 17088-0121 | Tablet, film coated | Drugs for further processing | March 17, 2016 |
| Everolimus | 17088-0247 | Tablet, for suspension | Drugs for further processing | August 29, 2012 |
| Everolimus | 17088-0114 | Tablet, for suspension | Drugs for further processing | August 29, 2012 |
| Everolimus | 17088-0107 | Tablet, for suspension | Drugs for further processing | August 29, 2012 |
| Everolimus | 17088-0261 | Tablet | Drugs for further processing | July 29, 2011 |
| Fingolimod hcl | 17088-0219 | Capsule | Drugs for further processing | September 21, 2010 |
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.