NDC 68001-671 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68001-671

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
BluePoint Laboratories
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
January 7, 2026
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (2)

Package NDCDescriptionSince
68001-671-00100 CAPSULE in 1 BOTTLE (68001-671-00)Jan 7, 2026
68001-671-081000 CAPSULE in 1 BOTTLE (68001-671-08)Jan 8, 2026

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