NDC 71335-1145 – Fluoxetine

Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1145

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
January 31, 2008
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
71335-1145-130 CAPSULE in 1 BOTTLE (71335-1145-1)May 24, 2019
71335-1145-260 CAPSULE in 1 BOTTLE (71335-1145-2)May 17, 2024
71335-1145-3100 CAPSULE in 1 BOTTLE (71335-1145-3)Mar 21, 2019
71335-1145-490 CAPSULE in 1 BOTTLE (71335-1145-4)Mar 12, 2019
71335-1145-528 CAPSULE in 1 BOTTLE (71335-1145-5)May 17, 2024
71335-1145-6180 CAPSULE in 1 BOTTLE (71335-1145-6)May 17, 2024
71335-1145-7120 CAPSULE in 1 BOTTLE (71335-1145-7)May 17, 2024

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