NDC 50228-421

Fluoxetine 20 mg tablet, film coated

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
Fluoxetine: every company that makes it
Form
tablet, film coated, oral
Strength
20 mg
Approval
ANDA ANDA210935
On the market since
Mar 20, 2019
Package NDCs
50228-421-01 50228-421-10 50228-421-30
Official label
DailyMed (National Library of Medicine), updated Oct 26, 2023

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