NDC 71335-1548 – Fluoxetine

Fluoxetine Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1548

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204597
Marketed since
March 16, 2015
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1548-130 CAPSULE in 1 BOTTLE (71335-1548-1)Jun 29, 2020
71335-1548-290 CAPSULE in 1 BOTTLE (71335-1548-2)Jul 24, 2020
71335-1548-360 CAPSULE in 1 BOTTLE (71335-1548-3)Jul 17, 2024
71335-1548-4120 CAPSULE in 1 BOTTLE (71335-1548-4)Jul 17, 2024
71335-1548-528 CAPSULE in 1 BOTTLE (71335-1548-5)Jul 17, 2024
71335-1548-615 CAPSULE in 1 BOTTLE (71335-1548-6)Jul 17, 2024
71335-1548-7100 CAPSULE in 1 BOTTLE (71335-1548-7)Jan 20, 2022
71335-1548-8180 CAPSULE in 1 BOTTLE (71335-1548-8)Jul 17, 2024

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