NDC 63629-1585 – Finasteride

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

Human Prescription Drug

Product NDC63629-1585

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, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (6)

Package NDCDescriptionSince
63629-1585-1100 TABLET, FILM COATED in 1 BOTTLE (63629-1585-1)Sep 9, 2026
63629-1585-230 TABLET, FILM COATED in 1 BOTTLE (63629-1585-2)Jun 3, 2011
63629-1585-360 TABLET, FILM COATED in 1 BOTTLE (63629-1585-3)Sep 4, 2012
63629-1585-490 TABLET, FILM COATED in 1 BOTTLE (63629-1585-4)Aug 16, 2012
63629-1585-5500 TABLET, FILM COATED in 1 BOTTLE (63629-1585-5)Sep 9, 2026
63629-1585-6180 TABLET, FILM COATED in 1 BOTTLE (63629-1585-6)Sep 9, 2026

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