NDC 57237-062 – Finasteride

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

Human Prescription Drug

Product NDC57237-062

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Rising Pharma Holdings, Inc.
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 (3)

Package NDCDescriptionSince
57237-062-05500 TABLET, FILM COATED in 1 BOTTLE (57237-062-05)Oct 30, 2007
57237-062-3030 TABLET, FILM COATED in 1 BOTTLE (57237-062-30)Oct 30, 2007
57237-062-9090 TABLET, FILM COATED in 1 BOTTLE (57237-062-90)Oct 30, 2007

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