NDC Code | 68151-3645-9 |
Package Description | 1 TABLET in 1 PACKAGE (68151-3645-9) |
Product NDC | 68151-3645 |
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 | ANDA090865 |
Manufacturer | Carilion Materials Management |
Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
Strength | 1 |
Strength Unit | mg/1 |
Pharmacy Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |