NDC 63187-265 – Finasteride

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

Human Prescription Drug

Product NDC63187-265

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Proficient Rx LP
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 (4)

Package NDCDescriptionSince
63187-265-1010 TABLET, FILM COATED in 1 BOTTLE (63187-265-10)Feb 11, 2022
63187-265-3030 TABLET, FILM COATED in 1 BOTTLE (63187-265-30)Nov 3, 2014
63187-265-6060 TABLET, FILM COATED in 1 BOTTLE (63187-265-60)Jul 3, 2017
63187-265-9090 TABLET, FILM COATED in 1 BOTTLE (63187-265-90)Jul 3, 2017

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