NDC 50436-4164

Diethylpropion Hydrochloride 25 mg tablet

On the label: Unit Dose Services. It's a repackaged product: Unit Dose Services rebottles it from KVK-TECH, Inc.'s NDC 10702-044.

Where the pills inside were made

Kvk-Tech, Inc.

Newtown, PA, United States · makes it

Serious problems, FDA action Last FDA inspection Mar 14, 2025. 13 inspections on record, 3 with serious problems.

Repackaging site

Product details

Generic drug
Diethylpropion: see every company that makes it
Form
tablet
Strength
25 mg
Approval
ANDA ANDA201212
On the market since
Dec 27, 2010
Package NDCs
50436-4164-1 50436-4164-5
Official label
DailyMed (National Library of Medicine), updated Jan 26, 2011

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