NDC 71656-089 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC71656-089

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Saptalis Pharmaceuticals, LLC.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA075525
Marketed since
June 20, 2025
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (1)

Package NDCDescriptionSince
71656-089-04120 mL in 1 BOTTLE (71656-089-04)Jun 20, 2025

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