NDC 10702-044

Diethylpropion Hydrochloride 25 mg tablet

On the label: KVK-TECH, Inc..

Where it's 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.

Product details

Generic drug
Diethylpropion: see every company that makes it
Form
tablet, oral
Strength
25 mg
Approval
ANDA ANDA201212
On the market since
Dec 27, 2010
Package NDCs
10702-044-01 10702-044-03 10702-044-06
Official label
DailyMed (National Library of Medicine), updated May 1, 2024

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