Data / Drug companies / Noven Therapeutics, LLC
Noven Therapeutics, LLC: 23 products in the FDA NDC directory, labeler code 68968
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Noven Therapeutics, LLC (labeler code 68968) lists 23 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 23 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on May 15, 2023.
The request: Watch Noven Therapeutics, LLC (FDA labeler code 68968): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 68968
- Products in commercial distribution
- 23
- Packages
- 26
- Finished drugs by generic name
- 5
- Prescription products
- 23
- Over the counter products
- 0
- Controlled substance products
- Schedule II 8
- Flagged as original packager
- 19 of 19 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- August 7, 1998
- 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) | 18 | 78.3% |
| Authorized generics (NDA) | 5 | 21.7% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 23 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Estradiol | 10 | 53 |
| Dextroamphetamine | 4 | 3 |
| Methylphenidate | 4 | 5 |
| Asenapine | 3 | 4 |
| Estradiol/norethindrone acetate transdermal system | 2 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Film, extended release | 13 | 56.5% |
| Patch, extended release | 6 | 26.1% |
| Patch | 4 | 17.4% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Estrogen | 12 |
| Central Nervous System Stimulant | 8 |
| Atypical Antipsychotic | 3 |
| Progestin | 2 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Xelstrym | 68968-0220 | Patch, extended release | New drug applications (NDA) | May 15, 2023 |
| Xelstrym | 68968-0215 | Patch, extended release | New drug applications (NDA) | May 15, 2023 |
| Xelstrym | 68968-0210 | Patch, extended release | New drug applications (NDA) | May 15, 2023 |
| Xelstrym | 68968-0205 | Patch, extended release | New drug applications (NDA) | May 15, 2023 |
| Secuado | 68968-0174 | Film, extended release | New drug applications (NDA) | February 12, 2020 |
| Secuado | 68968-0173 | Film, extended release | New drug applications (NDA) | February 12, 2020 |
| Secuado | 68968-0172 | Film, extended release | New drug applications (NDA) | February 12, 2020 |
| Estradiol | 68968-3475 | Film, extended release | Authorized generics (NDA) | January 1, 2018 |
| Estradiol | 68968-3450 | Film, extended release | Authorized generics (NDA) | January 1, 2018 |
| Estradiol | 68968-3437 | Film, extended release | Authorized generics (NDA) | January 1, 2018 |
| Estradiol | 68968-3425 | Film, extended release | Authorized generics (NDA) | January 1, 2018 |
| Estradiol | 68968-3410 | Film, extended release | Authorized generics (NDA) | January 1, 2018 |
| Minivelle | 68968-6675 | Film, extended release | New drug applications (NDA) | December 20, 2012 |
| Minivelle | 68968-6650 | Film, extended release | New drug applications (NDA) | December 20, 2012 |
| Minivelle | 68968-6637 | Film, extended release | New drug applications (NDA) | December 20, 2012 |
| Minivelle | 68968-6625 | Film, extended release | New drug applications (NDA) | December 20, 2012 |
| Minivelle | 68968-6610 | Film, extended release | New drug applications (NDA) | December 20, 2012 |
| Daytrana | 68968-5555 | Patch | New drug applications (NDA) | April 6, 2006 |
| Daytrana | 68968-5554 | Patch | New drug applications (NDA) | April 6, 2006 |
| Daytrana | 68968-5553 | Patch | New drug applications (NDA) | April 6, 2006 |
| Daytrana | 68968-5552 | Patch | New drug applications (NDA) | April 6, 2006 |
| CombiPatch (estradiol/norethindrone acetate transdermal system) | 68968-0525 | Patch, extended release | New drug applications (NDA) | August 7, 1998 |
| CombiPatch (estradiol/norethindrone acetate transdermal system) | 68968-0514 | Patch, extended release | New drug applications (NDA) | August 7, 1998 |
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.