NDC 68071-3819

Phentermine Hydrochloride 37.5 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare 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
68071-3819-1
Official label
DailyMed (National Library of Medicine), updated Mar 27, 2025

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