NDC 71335-1634 – Finasteride

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

Human Prescription Drug

Product NDC71335-1634

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090121
Marketed since
May 28, 2010
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
71335-1634-1100 TABLET, FILM COATED in 1 BOTTLE (71335-1634-1)Jun 10, 2020
71335-1634-230 TABLET, FILM COATED in 1 BOTTLE (71335-1634-2)Jun 10, 2020
71335-1634-360 TABLET, FILM COATED in 1 BOTTLE (71335-1634-3)Jun 10, 2020
71335-1634-490 TABLET, FILM COATED in 1 BOTTLE (71335-1634-4)Jun 10, 2020
71335-1634-5500 TABLET, FILM COATED in 1 BOTTLE (71335-1634-5)Jun 10, 2020
71335-1634-6180 TABLET, FILM COATED in 1 BOTTLE (71335-1634-6)Jun 10, 2020

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