| NDC Code | 62332-109-71 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-109-71) |
|---|
| Product NDC | 62332-109 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ropinirole |
|---|
| Non-Proprietary Name | Ropinirole |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200620 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202786 |
|---|
| Manufacturer | Alembic Pharmaceuticals Inc. |
|---|
| Substance Name | ROPINIROLE HYDROCHLORIDE |
|---|
| Strength | 6 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC] |
|---|