NDC Code | 64380-751-05 |
Package Description | 90 TABLET in 1 BOTTLE (64380-751-05) |
Product NDC | 64380-751 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Pramipexole Dihydrochloride |
Non-Proprietary Name | Pramipexole Dihydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20210215 |
Marketing Category Name | ANDA |
Application Number | ANDA202702 |
Manufacturer | Strides Pharma Science Limited |
Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
Strength | 1.5 |
Strength Unit | mg/1 |
Pharmacy Classes | Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC] |