NDC 71335-1898 – Finasteride

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

Human Prescription Drug

Product NDC71335-1898

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204304
Marketed since
January 5, 2017
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (6)

Package NDCDescriptionSince
71335-1898-1100 TABLET, FILM COATED in 1 BOTTLE (71335-1898-1)Aug 20, 2026
71335-1898-230 TABLET, FILM COATED in 1 BOTTLE (71335-1898-2)Oct 15, 2021
71335-1898-360 TABLET, FILM COATED in 1 BOTTLE (71335-1898-3)Nov 9, 2021
71335-1898-490 TABLET, FILM COATED in 1 BOTTLE (71335-1898-4)Jun 21, 2021
71335-1898-5500 TABLET, FILM COATED in 1 BOTTLE (71335-1898-5)Aug 20, 2026
71335-1898-6180 TABLET, FILM COATED in 1 BOTTLE (71335-1898-6)Aug 20, 2026

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