NDC 71610-699

Fluoxetine 20 mg capsule

On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from Radha Pharmaceuticals, Inc.'s NDC 77771-114.

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, oral
Strength
20 mg
Approval
ANDA ANDA204597
On the market since
Oct 24, 2022
Package NDCs
71610-699-30 71610-699-53 71610-699-60 71610-699-70 71610-699-80 71610-699-92
Official label
DailyMed (National Library of Medicine), updated Apr 5, 2023

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