NDC 51655-100 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC51655-100

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
May 20, 2014
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (2)

Package NDCDescriptionSince
51655-100-2690 CAPSULE in 1 BOTTLE, PLASTIC (51655-100-26)Aug 30, 2022
51655-100-5230 CAPSULE in 1 BOTTLE, DISPENSING (51655-100-52)May 20, 2014

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