NDC 71656-089

Fluoxetine 20 mg per 5 mL solution

On the label: Saptalis Pharmaceuticals, LLC..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Saptalis Pharmaceuticals LLCHauppauge, NY, United StatesMakes it Problems found, fixed voluntarilyMar 6, 2026 · 4 inspections

Product details

Generic drug
Fluoxetine: every company that makes it
Form
solution, oral
Strength
20 mg per 5 mL
Approval
ANDA ANDA075525
On the market since
Jun 20, 2025
Package NDCs
71656-089-04
Official label
DailyMed (National Library of Medicine), updated Jun 23, 2025

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?