
USFDA APPLICATION NUMBER - 20667 / DOSAGE - TABLET;ORAL - 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| pramipexole dihydrochloride(UNII: 3D867NP06J) (pramipexole - UNII:83619PEU5T) | pramipexole dihydrochloride | 0.250mg |
Inactive Ingredients
| Ingredient Name | Boehringer Ingelheim Pharmaceuticals, Inc. | Cardinal Health | Lake Erie Medical DBA Quality Care Products LLC |
|---|---|---|---|
| MAGNESIUM STEARATE(70097M6I30) | |||
| mannitol(3OWL53L36A) | |||
| POVIDONE(FZ989GH94E) | |||
| POVIDONES(FZ989GH94E) | |||
| silicon dioxide(ETJ7Z6XBU4) | |||
| starch, corn(O8232NY3SJ) |