NDC 17856-0090 – Finasteride

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

Human Prescription Drug

Product NDC17856-0090

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Atlantic Biologicals Corps
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 (1)

Package NDCDescriptionSince
17856-0090-11 TABLET, FILM COATED in 1 POUCH (17856-0090-1)Jan 11, 2021

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