NDC 50228-422 – Fluoxetine

Fluoxetine Hydrochloride 60 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50228-422

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211282
Marketed since
January 10, 2019
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (2)

Package NDCDescriptionSince
50228-422-101000 TABLET in 1 BOTTLE (50228-422-10)Jan 10, 2019
50228-422-3030 TABLET in 1 BOTTLE (50228-422-30)Jan 10, 2019

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