| NDC Code | 54868-6237-0 |
|---|
| Package Description | 63 TABLET in 1 BOTTLE (54868-6237-0) |
|---|
| Product NDC | 54868-6237 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pramipexole Dihydrochloride |
|---|
| Non-Proprietary Name | Pramipexole Dihydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110408 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077724 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
|---|
| Strength | .125 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
|---|