NDC Code | 13668-092-74 |
Package Description | 100 TABLET in 1 CARTON (13668-092-74) |
Product NDC | 13668-092 |
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 | Torrent Pharmaceuticals Limited |
Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
Strength | .25 |
Strength Unit | mg/1 |
Pharmacy Classes | Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC] |