NDC 68999-730 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/5mL · Liquid · Oral

Human Prescription Drug

Product NDC68999-730

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Chartwell Governmental & Specialty RX, LLC
Dosage form
Liquid
Route
Oral
Marketing category
ANDA · ANDA076458
Marketed since
May 14, 2004
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (1)

Package NDCDescriptionSince
68999-730-242 TRAY in 1 BOX (68999-730-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-730-45)Oct 31, 2025

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