Register entry
- Registered sites
- 0
- Active NDC listings
- 6
- Labeller names
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
66 active NDC listings: 6 human prescription drug. By marketing category: NDA 6.
| Dosage form | NDCs |
|---|---|
| tablet, film coated | 3 |
| tablet | 2 |
| kit | 1 |
| Route | NDCs |
|---|---|
| oral | 5 |
| Labeller name on the listing | NDCs |
|---|---|
| taiho pharmaceutical co., ltd. | 3 |
| taiho pharmaceutical co., ltd. | 3 |
Catalogue
Marketed products
6| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| INQOVI | CEDAZURIDINE and DECITABINE | tablet, film coated, oral | 64842-0727NDA |
| LONSURF | trifluridine and tipiracil | tablet, film coated, oral | 64842-1020NDA |
| LONSURF | trifluridine and tipiracil | tablet, film coated, oral | 64842-1025NDA |
| LYTGOBI | FUTIBATINIB | tablet, oral | 64842-0120NDA |
| LYTGOBI | FUTIBATINIB | tablet, oral | 64842-0127NDA |
| LYTGOBI | LYTGOBI | kit | 64842-0128NDA |
Compare
Other companies listing futibatinib
- PENN PHARMACEUTICALS LIMITED1 site · 24 NDC
Enquiry
Common questions
- Is Taiho Pharmaceutical Co., Ltd. FDA approved?
- Taiho Pharmaceutical Co., Ltd. holds no registered establishment of its own; 6 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Taiho Pharmaceutical Co., Ltd. make?
- 6 products are listed under Taiho Pharmaceutical Co., Ltd. in the openFDA NDC Directory, most often as tablet, film coated; tablet; kit. 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.