Fluoxetine 71656-0089-04

Package NDC

71656-0089-04

Manufacturer: Saptalis Pharmaceuticals, Llc.
Dosage Form: Solution
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 20, 2025
Listing Expires: December 31, 2026
Application: ANDA075525

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Active Ingredients

Ingredient	Strength
Fluoxetine Hydrochloride	20 mg/5mL

Drug Class

Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]

Selected Package

71656-0089-04Selected

120 mL in 1 BOTTLE (71656-089-04)