NDC 67296-1568

Fluoxetine 20 mg capsule

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Vensun Pharmaceuticals, Inc.'s NDC 42543-726.

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
Fluoxetine: every company that makes it
Form
capsule
Strength
20 mg
Approval
ANDA ANDA204597
On the market since
Mar 16, 2015
Package NDCs
67296-1568-3
Official label
DailyMed (National Library of Medicine), updated Jan 21, 2022

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