NDC 71335-2784 – Fluoxetine

Fluoxetine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2784

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213286
Marketed since
April 8, 2020
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (2)

Package NDCDescriptionSince
71335-2784-130 TABLET, FILM COATED in 1 BOTTLE (71335-2784-1)Aug 18, 2025
71335-2784-2100 TABLET, FILM COATED in 1 BOTTLE (71335-2784-2)Aug 18, 2025

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