Register entry
- Registered sites
- 0
- Active NDC listings
- 22
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
2222 active NDC listings: 22 bulk ingredient. By marketing category: BULK INGREDIENT 22.
| Dosage form | NDCs |
|---|---|
| powder | 16 |
| liquid | 4 |
| solution | 2 |
| Route | NDCs |
|---|
| Labeller name on the listing | NDCs |
|---|---|
| eli lilly kinsale limited | 22 |
Catalogue
Marketed products
22| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Abemaciclib | powder | 63419-0554BULK INGREDIENT |
| - | Abemaciclib | powder | 63419-0578BULK INGREDIENT |
| - | Atomoxetine hydrochloride | powder | 63419-0440BULK INGREDIENT |
| - | Baricitinib | powder | 63419-0552BULK INGREDIENT |
| - | DULAGLUTIDE | solution | 63419-0525BULK INGREDIENT |
| - | Donanemab | liquid | 63419-0874BULK INGREDIENT |
| - | Imlunestrant | powder | 63419-0264BULK INGREDIENT |
| - | Ixekizumab | solution | 63419-0536BULK INGREDIENT |
| - | Lasmiditan hemisuccinate | powder | 63419-0576BULK INGREDIENT |
| - | Lasmiditan hemisuccinate | powder | 63419-0580BULK INGREDIENT |
| - | Mirikizumab | liquid | 63419-0573BULK INGREDIENT |
| - | Olanzapine | powder | 63419-0402BULK INGREDIENT |
| - | Olanzapine pamoate monohydrate | powder | 63419-0509BULK INGREDIENT |
| - | Orforglipron | powder | 63419-0603BULK INGREDIENT |
| - | Pemetrexed Disodium Heptahydrate | powder | 63419-0449BULK INGREDIENT |
| - | Pemetrexed Disodium Heptahydrate | powder | 63419-0533BULK INGREDIENT |
| - | Pirtobrutinib | powder | 63419-0739BULK INGREDIENT |
| - | RAMUCIRUMAB | liquid | 63419-0535BULK INGREDIENT |
| - | Raloxifene hydrochloride | powder | 63419-0420BULK INGREDIENT |
| - | Selpercatinib | powder | 63419-0597BULK INGREDIENT |
| - | Selpercatinib | powder | 63419-0681BULK INGREDIENT |
| - | insulin efsitora alfa | liquid | 63419-0184BULK INGREDIENT |
Compare
Other companies listing abemaciclib
- Lonza Biologics Inc15 sites · 80 NDC
- MSN Laboratories Private Limited,8 sites · 275 NDC
- Hetero Labs Limited8 sites · 167 NDC
- SciAnda (Changshu) Pharmaceuticals, Ltd.1 site · 16 NDC
- Porton Pharma Solutions Ltd1 site · 10 NDC
Enquiry
Common questions
- Is Eli Lilly Kinsale Limited FDA approved?
- Eli Lilly Kinsale Limited holds no registered establishment of its own; 22 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Eli Lilly Kinsale Limited make?
- 22 products are listed under Eli Lilly Kinsale Limited in the openFDA NDC Directory, most often as powder; liquid; solution. 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.