Strength
.75 mg/1
Manufacturer
Aurobindo Pharma LimitedNDC
65862060790
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
2/22/2017
Active Ingredients
PRAMIPEXOLE DIHYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA202633On Market Since
10/26/2012
Pharmacological Classes
Dopamine Agonists
Nonergot Dopamine Agonist
PRAMIPEXOLE 0.75 MG TABLET
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