NDC 42543-709

Pramipexole Dihydrochloride 1.5 mg tablet

On the label: Vensun Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it and tests 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
Strength
1.5 mg
Approval
ANDA ANDA203855
On the market since
Oct 29, 2014
Package NDCs
42543-709-05 42543-709-10 42543-709-90
Official label
DailyMed (National Library of Medicine), updated Aug 8, 2018

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