NDC 71335-1482 – Fluoxetine

Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1482

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, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (7)

Package NDCDescriptionSince
71335-1482-130 CAPSULE in 1 BOTTLE (71335-1482-1)Feb 12, 2020
71335-1482-260 CAPSULE in 1 BOTTLE (71335-1482-2)Feb 18, 2021
71335-1482-3100 CAPSULE in 1 BOTTLE (71335-1482-3)Apr 21, 2020
71335-1482-490 CAPSULE in 1 BOTTLE (71335-1482-4)Jan 17, 2020
71335-1482-528 CAPSULE in 1 BOTTLE (71335-1482-5)Jul 15, 2024
71335-1482-6180 CAPSULE in 1 BOTTLE (71335-1482-6)Jul 15, 2024
71335-1482-7120 CAPSULE in 1 BOTTLE (71335-1482-7)Jul 15, 2024

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