NDC 55289-701

Phentermine Hydrochloride 37.5 mg tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-025.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Repackaging site

Product details

Generic drug
Phentermine: every company that makes it
Form
tablet, oral
Strength
37.5 mg
Approval
ANDA ANDA040876
On the market since
Aug 15, 2012
Package NDCs
55289-701-07 55289-701-14 55289-701-15 55289-701-21 55289-701-28 55289-701-30 55289-701-32 55289-701-42 55289-701-45 55289-701-56 55289-701-60 55289-701-90
Official label
DailyMed (National Library of Medicine), updated Oct 20, 2025

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