NDC 71335-1048 – Fluoxetine

Fluoxetine Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1048

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 (8)

Package NDCDescriptionSince
71335-1048-130 CAPSULE in 1 BOTTLE (71335-1048-1)Jan 25, 2019
71335-1048-290 CAPSULE in 1 BOTTLE (71335-1048-2)Dec 31, 2018
71335-1048-360 CAPSULE in 1 BOTTLE (71335-1048-3)May 17, 2024
71335-1048-4120 CAPSULE in 1 BOTTLE (71335-1048-4)May 17, 2024
71335-1048-528 CAPSULE in 1 BOTTLE (71335-1048-5)May 17, 2024
71335-1048-615 CAPSULE in 1 BOTTLE (71335-1048-6)May 17, 2024
71335-1048-7100 CAPSULE in 1 BOTTLE (71335-1048-7)May 17, 2024
71335-1048-8180 CAPSULE in 1 BOTTLE (71335-1048-8)May 17, 2024

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