NDC 72189-542 – Finasteride

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

Human Prescription Drug

Product NDC72189-542

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204304
Marketed since
March 11, 2024
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (2)

Package NDCDescriptionSince
72189-542-3030 TABLET, FILM COATED in 1 BOTTLE (72189-542-30)Mar 11, 2024
72189-542-9090 TABLET, FILM COATED in 1 BOTTLE (72189-542-90)Mar 11, 2024

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