NDC 71335-2020 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2020

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 (9)

Package NDCDescriptionSince
71335-2020-130 CAPSULE in 1 BOTTLE (71335-2020-1)Jan 24, 2022
71335-2020-2100 CAPSULE in 1 BOTTLE (71335-2020-2)Jan 24, 2023
71335-2020-360 CAPSULE in 1 BOTTLE (71335-2020-3)Dec 22, 2021
71335-2020-415 CAPSULE in 1 BOTTLE (71335-2020-4)Jul 15, 2024
71335-2020-556 CAPSULE in 1 BOTTLE (71335-2020-5)Jul 15, 2024
71335-2020-628 CAPSULE in 1 BOTTLE (71335-2020-6)Jul 15, 2024
71335-2020-790 CAPSULE in 1 BOTTLE (71335-2020-7)Jan 18, 2022
71335-2020-8120 CAPSULE in 1 BOTTLE (71335-2020-8)Jul 15, 2024
71335-2020-945 CAPSULE in 1 BOTTLE (71335-2020-9)Jul 15, 2024

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