NDC 50090-5101

Bupropion Hydrochloride (SR) 150 mg tablet, extended release

On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-863.

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, extended release, oral
Strength
150 mg
Approval
ANDA ANDA206122
On the market since
Aug 17, 2016
Package NDCs
50090-5101-0 50090-5101-1
Official label
DailyMed (National Library of Medicine), updated Jul 9, 2025

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