NDC 71335-1702

Bupropion Hydrochloride SR 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 50228-175.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it and tests 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 ANDA205794
On the market since
Apr 20, 2018
Package NDCs
71335-1702-1 71335-1702-2 71335-1702-3 71335-1702-4 71335-1702-5 71335-1702-6 71335-1702-7 71335-1702-8 71335-1702-9
Official label
DailyMed (National Library of Medicine), updated May 14, 2026

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