NDC 82009-102 – Fluoxetine

Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC82009-102

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
QUALLENT PHARMACEUTICALS HEALTH LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
September 1, 2023
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
82009-102-05500 CAPSULE in 1 BOTTLE (82009-102-05)Sep 1, 2023

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