NDC 71205-393 – Fluoxetine

Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71205-393

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
Proficient Rx LP
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 (3)

Package NDCDescriptionSince
71205-393-3030 CAPSULE in 1 BOTTLE (71205-393-30)Feb 3, 2020
71205-393-6060 CAPSULE in 1 BOTTLE (71205-393-60)Feb 3, 2020
71205-393-9090 CAPSULE in 1 BOTTLE (71205-393-90)Feb 3, 2020

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