NDC 50228-420 – Fluoxetine

Fluoxetine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50228-420

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
ScieGen Pharmaceuticals, Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210935
Marketed since
March 20, 2019
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (3)

Package NDCDescriptionSince
50228-420-01100 TABLET, FILM COATED in 1 BOTTLE (50228-420-01)Mar 20, 2019
50228-420-101000 TABLET, FILM COATED in 1 BOTTLE (50228-420-10)Mar 20, 2019
50228-420-3030 TABLET, FILM COATED in 1 BOTTLE (50228-420-30)Mar 20, 2019

Other Fluoxetine products