NDC 43063-541

Benzphetamine Hydrochloride 50 mg tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-040.

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
Benzphetamine: every company that makes it
Form
tablet, oral
Strength
50 mg
Approval
ANDA ANDA090968
On the market since
Jul 21, 2010
Package NDCs
43063-541-14 43063-541-30 43063-541-45 43063-541-60 43063-541-90 43063-541-98
Official label
DailyMed (National Library of Medicine), updated Sep 23, 2026

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