NDC 76420-151 – Finasteride

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

Human Prescription Drug

Product NDC76420-151

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203687
Marketed since
November 5, 2013
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
76420-151-3030 TABLET, FILM COATED in 1 BOTTLE (76420-151-30)Jan 18, 2022
76420-151-9090 TABLET, FILM COATED in 1 BOTTLE (76420-151-90)Jan 18, 2022

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