NDC 71335-0923 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0923

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 (9)

Package NDCDescriptionSince
71335-0923-130 CAPSULE in 1 BOTTLE (71335-0923-1)Aug 9, 2018
71335-0923-2100 CAPSULE in 1 BOTTLE (71335-0923-2)Aug 9, 2018
71335-0923-360 CAPSULE in 1 BOTTLE (71335-0923-3)Aug 9, 2018
71335-0923-415 CAPSULE in 1 BOTTLE (71335-0923-4)Aug 9, 2018
71335-0923-556 CAPSULE in 1 BOTTLE (71335-0923-5)Aug 9, 2018
71335-0923-628 CAPSULE in 1 BOTTLE (71335-0923-6)Aug 9, 2018
71335-0923-790 CAPSULE in 1 BOTTLE (71335-0923-7)Aug 9, 2018
71335-0923-8120 CAPSULE in 1 BOTTLE (71335-0923-8)Aug 9, 2018
71335-0923-945 CAPSULE in 1 BOTTLE (71335-0923-9)Aug 9, 2018

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