| NDC Code | 29300-270-19 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (29300-270-19) |
|---|
| Product NDC | 29300-270 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pramipexole Dihydrochloride |
|---|
| Non-Proprietary Name | Pramipexole Dihydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190301 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207011 |
|---|
| Manufacturer | Unichem Pharmaceuticals (USA), Inc. |
|---|
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
|---|
| Strength | .75 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC] |
|---|