NDC 57237-182

Pramipexole Dihydrochloride 0.5 mg tablet

On the label: Rising Pharma Holdings, Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Pramipexole: every company that makes it
Form
tablet, oral
Strength
0.5 mg
Approval
ANDA ANDA202633
On the market since
Oct 26, 2012
Package NDCs
57237-182-90 57237-182-99
Official label
DailyMed (National Library of Medicine), updated Dec 11, 2025

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