NDC 71335-1033 – Fluoxetine

Fluoxetine Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1033

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 (7)

Package NDCDescriptionSince
71335-1033-130 CAPSULE in 1 BOTTLE (71335-1033-1)Jan 3, 2019
71335-1033-290 CAPSULE in 1 BOTTLE (71335-1033-2)Jan 3, 2019
71335-1033-360 CAPSULE in 1 BOTTLE (71335-1033-3)Jan 3, 2019
71335-1033-4120 CAPSULE in 1 BOTTLE (71335-1033-4)Jan 3, 2019
71335-1033-528 CAPSULE in 1 BOTTLE (71335-1033-5)Jan 3, 2019
71335-1033-615 CAPSULE in 1 BOTTLE (71335-1033-6)Jan 3, 2019
71335-1033-7100 CAPSULE in 1 BOTTLE (71335-1033-7)Jan 3, 2019

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