NDC 71335-0827 – Fluoxetine

Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0827

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
71335-0827-130 CAPSULE in 1 BOTTLE (71335-0827-1)Jun 29, 2016
71335-0827-260 CAPSULE in 1 BOTTLE (71335-0827-2)Jun 29, 2016
71335-0827-3100 CAPSULE in 1 BOTTLE (71335-0827-3)Jun 29, 2016
71335-0827-490 CAPSULE in 1 BOTTLE (71335-0827-4)Jun 29, 2016
71335-0827-528 CAPSULE in 1 BOTTLE (71335-0827-5)Jun 29, 2016
71335-0827-6180 CAPSULE in 1 BOTTLE (71335-0827-6)Jun 29, 2016
71335-0827-7120 CAPSULE in 1 BOTTLE (71335-0827-7)Jun 29, 2016

Other Fluoxetine products