NDC Code | 54868-4912-1 |
Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-4912-1) |
Product NDC | 54868-4912 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Mirapex |
Non-Proprietary Name | Pramipexole Dihydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20030904 |
Marketing Category Name | NDA |
Application Number | NDA020667 |
Manufacturer | Physicians Total Care, Inc. |
Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
Strength | .125 |
Strength Unit | mg/1 |
Pharmacy Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |