NDC 72789-278

Minoxidil 2.5 mg tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 53489-386.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Frontida BioPharm, LLCPhiladelphia, PA, United StatesMakes it No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Minoxidil: every company that makes it
Form
tablet, oral
Strength
2.5 mg
Approval
ANDA ANDA072709
On the market since
Dec 14, 1995
Package NDCs
72789-278-01
Official label
DailyMed (National Library of Medicine), updated Jul 17, 2026

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