NDC 72162-1526

Bupropion Hydrochloride(XL) 150 mg tablet, film coated, extended release

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-144.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it and labels it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Bupropion: every company that makes it
Form
tablet, film coated, extended release, oral
Strength
150 mg
Approval
ANDA ANDA207479
On the market since
Apr 12, 2017
Package NDCs
72162-1526-3 72162-1526-5
Official label
DailyMed (National Library of Medicine), updated May 28, 2026

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