Register entry
- Registered sites
- 0
- Active NDC listings
- 3
- Live patents
- 6
- Countries
- 0
Catalogue
Drug listings by form and route
33 active NDC listings: 3 human prescription drug. By marketing category: NDA 2, ANDA 1.
| Dosage form | NDCs |
|---|---|
| tablet, extended release | 2 |
| tablet | 1 |
| Route | NDCs |
|---|---|
| oral | 3 |
| Labeller name on the listing | NDCs |
|---|---|
| tripoint therapeutics, llc | 3 |
Exclusivity
Patents and exclusivities
6| Patent | Product | Covers | Expiry |
|---|---|---|---|
| 8163306 | ELEPSIA XRlevetiracetam | product | Sept 2027 |
| 8431156 | ELEPSIA XRlevetiracetam | product | Oct 2027 |
| 8470367 | ELEPSIA XRlevetiracetam | product | Oct 2027 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Carbinoxamine Maleate | Carbinoxamine Maleate | tablet, oral | 80705-120ANDA |
| ELEPSIA XR 1000 MG | levetiracetam | tablet, extended release, oral | 80705-100NDA |
| ELEPSIA XR 1500 MG | levetiracetam | tablet, extended release, oral | 80705-101NDA |
Compare
Other companies listing levetiracetam
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- Baxter Healthcare Corporation16 sites · 416 NDC
- Fresenius Kabi USA, LLC6 sites · 561 NDC
- ScieGen Pharmaceuticals India Private Limited3 sites · 200 NDC
- Safecor Health, LLC3 sites · 103 NDC
- UCB, Inc.2 sites · 65 NDC
- Bryant Ranch Prepack1 site · 4,357 NDC
- Precision Dose Inc.1 site · 76 NDC
- Aprecia Pharmaceuticals, LLC1 site · 4 NDC
- MAJOR Pharmaceuticals Inc.0 sites · 619 NDC
Enquiry
Common questions
- Is TRIPOINT THERAPEUTICS, LLC FDA approved?
- TRIPOINT THERAPEUTICS, LLC holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does TRIPOINT THERAPEUTICS, LLC make?
- 3 products are listed under TRIPOINT THERAPEUTICS, LLC in the openFDA NDC Directory, most often as tablet, extended release; tablet. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.