NDC 50228-176

Bupropion Hydrochloride SR 200 mg tablet, film coated, extended release

On the label: ScieGen Pharmaceuticals, Inc..

United States: 1

Where it's 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

Product details

Generic drug
Bupropion: every company that makes it
Form
tablet, film coated, extended release, oral
Strength
200 mg
Approval
ANDA ANDA205794
On the market since
Apr 20, 2018
Package NDCs
50228-176-01 50228-176-10 50228-176-30 50228-176-60
Official label
DailyMed (National Library of Medicine), updated Oct 8, 2026

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