NDC 62332-157

Pramipexole Dihydrochloride 2.25 mg tablet, extended release

On the label: Alembic Pharmaceuticals Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Alembic Pharmaceuticals LimitedPanchmahal, IndiaMakes it No problems foundJul 26, 2024 · 8 inspections

Product details

Generic drug
Pramipexole: every company that makes it
Form
tablet, extended release, oral
Strength
2.25 mg
Approval
ANDA ANDA204518
On the market since
Jan 3, 2019
Package NDCs
62332-157-30
Official label
DailyMed (National Library of Medicine), updated Jun 20, 2024

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