NDC 31722-907

Pramipexole 0.25 mg tablet

On the label: Camber Pharmaceuticals Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Pramipexole: every company that makes it
Form
tablet, oral
Strength
0.25 mg
Approval
ANDA ANDA203855
On the market since
Aug 1, 2015
Package NDCs
31722-907-05 31722-907-10 31722-907-90
Official label
DailyMed (National Library of Medicine), updated Oct 13, 2016

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