NDC 42708-200 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC42708-200

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
QPharma Inc
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
July 11, 2025
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
42708-200-30 sample30 CAPSULE in 1 BOTTLE, PLASTIC (42708-200-30)Jun 8, 2026

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