NDC 71335-1530 – Finasteride

Finasteride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1530

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078341
Marketed since
October 30, 2007
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (6)

Package NDCDescriptionSince
71335-1530-1100 TABLET, FILM COATED in 1 BOTTLE (71335-1530-1)Dec 28, 2021
71335-1530-230 TABLET, FILM COATED in 1 BOTTLE (71335-1530-2)Mar 6, 2020
71335-1530-360 TABLET, FILM COATED in 1 BOTTLE (71335-1530-3)Dec 28, 2021
71335-1530-490 TABLET, FILM COATED in 1 BOTTLE (71335-1530-4)Mar 20, 2020
71335-1530-5500 TABLET, FILM COATED in 1 BOTTLE (71335-1530-5)Dec 28, 2021
71335-1530-6180 TABLET, FILM COATED in 1 BOTTLE (71335-1530-6)Dec 28, 2021

Other Finasteride products