NDC 0904-6704

Pramipexole Dihydrochloride 0.25 mg tablet

On the label: Major Pharmaceuticals. It's repackaged: Major Pharmaceuticals rebottles it from Torrent Pharma, Inc.'s NDC 13668-092.

India: 2

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Torrent Pharmaceuticals LimitedIndrad, IndiaMakes it Problems found, fixed voluntarilyJun 12, 2024 · 7 inspections, 2 with FDA action
Torrent Pharmaceuticals LimitedBharuch, IndiaMakes it, tests it and packages it No problems foundJan 23, 2026 · 5 inspections, 1 with FDA action

Product details

Generic drug
Pramipexole: every company that makes it
Form
tablet, oral
Strength
0.25 mg
Approval
ANDA ANDA090865
On the market since
Oct 8, 2010
Package NDCs
0904-6704-61
Official label
DailyMed (National Library of Medicine), updated Jan 21, 2026

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