| NDC Code | 0378-1711-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (0378-1711-05) |
|---|
| Product NDC | 0378-1711 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pramipexole Dihydrochloride |
|---|
| Non-Proprietary Name | Pramipexole Dihydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101104 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077854 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
|---|