NDC 31722-904

Fluoxetine 20 mg capsule

On the label: Camber Pharmaceuticals Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Fluoxetine: every company that makes it
Form
capsule
Strength
20 mg
Approval
ANDA ANDA204597
On the market since
Jul 30, 2015
Package NDCs
31722-904-01 31722-904-05 31722-904-10 31722-904-30
Official label
DailyMed (National Library of Medicine), updated Apr 28, 2017

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