NDC 72189-586

Quetiapine Fumarate ER 150 mg tablet, film coated, extended release

On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-381.

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
Quetiapine: every company that makes it
Form
tablet, film coated, extended release, oral
Strength
150 mg
Approval
ANDA ANDA209635
On the market since
Oct 2, 2024
Package NDCs
72189-586-30
Official label
DailyMed (National Library of Medicine), updated Oct 2, 2024

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