| NDC Code | 68462-333-11 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (68462-333-11) / 10 TABLET in 1 BLISTER PACK |
|---|
| Product NDC | 68462-333 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pramipexole Dihydrochloride |
|---|
| Non-Proprietary Name | Pramipexole Dihydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101008 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090781 |
|---|
| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
|---|
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC] |
|---|