NDC 42708-182 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC42708-182

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
QPharma Inc
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
January 31, 2008
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
42708-182-30 sample30 CAPSULE in 1 BOTTLE, PLASTIC (42708-182-30)May 26, 2023

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