Register entry
- Registered sites
- 0
- Active NDC listings
- 26
- Labeller names
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
2626 active NDC listings: 26 human prescription drug. By marketing category: ANDA 26.
| Dosage form | NDCs |
|---|---|
| capsule | 13 |
| tablet, film coated | 5 |
| tablet, orally disintegrating | 5 |
| tablet | 3 |
| Route | NDCs |
|---|---|
| oral | 26 |
| Labeller name on the listing | NDCs |
|---|---|
| amerisyn llc | 18 |
| amerisyn, llc | 8 |
Catalogue
Marketed products
26| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| DICLOFENAC POTASSIUM | diclofenac potassium, film coated | tablet, oral | 87564-011ANDA |
| Eltrombopag olamine | Eltrombopag olamine | tablet, film coated, oral | 87564-032ANDA |
| Eltrombopag olamine | Eltrombopag olamine | tablet, film coated, oral | 87564-033ANDA |
| Eltrombopag olamine | Eltrombopag olamine | tablet, film coated, oral | 87564-034ANDA |
| Eltrombopag olamine | Eltrombopag olamine | tablet, film coated, oral | 87564-035ANDA |
| KETOCONAZOLE | ketoconazole | tablet, oral | 87564-051ANDA |
| Ketorolac Tromethamine | ketorolac tromethamine | tablet, film coated, oral | 87564-018ANDA |
| MEXILETINE HYDROCHLORIDE | mexiletine hydrochloride | capsule, oral | 87564-052ANDA |
| MEXILETINE HYDROCHLORIDE | mexiletine hydrochloride | capsule, oral | 87564-053ANDA |
| MEXILETINE HYDROCHLORIDE | mexiletine hydrochloride | capsule, oral | 87564-054ANDA |
| NICARDIPINE HYDROCHLORIDE | nicardipine hydrochloride | capsule, oral | 87564-027ANDA |
| NICARDIPINE HYDROCHLORIDE | nicardipine hydrochloride | capsule, oral | 87564-028ANDA |
| RISPERIDONE | RISPERIDONE | tablet, orally disintegrating, oral | 87564-013ANDA |
| RISPERIDONE | RISPERIDONE | tablet, orally disintegrating, oral | 87564-014ANDA |
| RISPERIDONE | RISPERIDONE | tablet, orally disintegrating, oral | 87564-015ANDA |
| RISPERIDONE | RISPERIDONE | tablet, orally disintegrating, oral | 87564-016ANDA |
| RISPERIDONE | RISPERIDONE | tablet, orally disintegrating, oral | 87564-017ANDA |
| TERAZOSIN HYDROCHLORIDE | terazosin hydrochloride | capsule, oral | 87564-081ANDA |
| TERAZOSIN HYDROCHLORIDE | terazosin hydrochloride | capsule, oral | 87564-082ANDA |
| TERAZOSIN HYDROCHLORIDE | terazosin hydrochloride | capsule, oral | 87564-083ANDA |
| TERAZOSIN HYDROCHLORIDE | terazosin hydrochloride | capsule, oral | 87564-084ANDA |
| TERBINAFINE | terbinafine hydrochloride tablet | tablet, oral | 87564-010ANDA |
| Terazosin Hydrochloride | Terazosin Hydrochloride | capsule, oral | 87564-006ANDA |
| Terazosin Hydrochloride | Terazosin Hydrochloride | capsule, oral | 87564-007ANDA |
| Terazosin Hydrochloride | Terazosin Hydrochloride | capsule, oral | 87564-008ANDA |
| Terazosin Hydrochloride | Terazosin Hydrochloride | capsule, oral | 87564-009ANDA |
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Enquiry
Common questions
- Is Amerisyn, LLC FDA approved?
- Amerisyn, LLC holds no registered establishment of its own; 26 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Amerisyn, LLC make?
- 26 products are listed under Amerisyn, LLC in the openFDA NDC Directory, most often as capsule; tablet, film coated; tablet, orally disintegrating. 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.