NDC 33342-208

Pramipexole Dihydrochloride 0.375 mg tablet, extended release

On the label: Macleods Pharmaceuticals Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedDistrict Solan, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action

Product details

Generic drug
Pramipexole: every company that makes it
Form
tablet, extended release, oral
Strength
0.375 mg
Approval
ANDA ANDA206156
On the market since
Aug 24, 2020
Package NDCs
33342-208-07 33342-208-12
Official label
DailyMed (National Library of Medicine), updated Jul 6, 2024

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