Strength
3 mg/1
Manufacturer
NorthStar Rx LLCNDC
16714092001
Classification
Generic
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
PRAMIPEXOLE DIHYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA206156On Market Since
3/6/2019
Pharmacological Classes
Dopamine Agonists
Nonergot Dopamine Agonist
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