NDC 43063-712 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC43063-712

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
January 31, 2008
Marketing end
November 30, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (4)

Package NDCDescriptionSince
43063-712-2121 CAPSULE in 1 BOTTLE, PLASTIC (43063-712-21)Jan 31, 2017
43063-712-3030 CAPSULE in 1 BOTTLE, PLASTIC (43063-712-30)Oct 3, 2016
43063-712-6060 CAPSULE in 1 BOTTLE, PLASTIC (43063-712-60)Aug 24, 2018
43063-712-9090 CAPSULE in 1 BOTTLE, PLASTIC (43063-712-90)Jan 31, 2017

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