NDC 71335-0924 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0924

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA076001
Marketed since
January 29, 2002
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
71335-0924-130 CAPSULE in 1 BOTTLE (71335-0924-1)Aug 31, 2018
71335-0924-2100 CAPSULE in 1 BOTTLE (71335-0924-2)Dec 14, 2018
71335-0924-360 CAPSULE in 1 BOTTLE (71335-0924-3)Apr 5, 2019
71335-0924-415 CAPSULE in 1 BOTTLE (71335-0924-4)Sep 21, 2022
71335-0924-556 CAPSULE in 1 BOTTLE (71335-0924-5)Sep 21, 2022
71335-0924-628 CAPSULE in 1 BOTTLE (71335-0924-6)Sep 21, 2022
71335-0924-790 CAPSULE in 1 BOTTLE (71335-0924-7)Sep 5, 2018
71335-0924-8120 CAPSULE in 1 BOTTLE (71335-0924-8)Sep 21, 2022
71335-0924-945 CAPSULE in 1 BOTTLE (71335-0924-9)Sep 21, 2022

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