NDC 65862-605

Pramipexole Dihydrochloride 0.25 mg tablet

On the label: Aurobindo Pharma Limited.

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
0.25 mg
Approval
ANDA ANDA202633
On the market since
Oct 26, 2012
Package NDCs
65862-605-10 65862-605-78 65862-605-90 65862-605-99
Official label
DailyMed (National Library of Medicine), updated Oct 3, 2025

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