NDC 50090-4697 – Finasteride

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

Human Prescription Drug

Product NDC50090-4697

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204304
Marketed since
January 5, 2017
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (3)

Package NDCDescriptionSince
50090-4697-030 TABLET, FILM COATED in 1 BOTTLE (50090-4697-0)Nov 7, 2019
50090-4697-190 TABLET, FILM COATED in 1 BOTTLE (50090-4697-1)Nov 7, 2019
50090-4697-2100 TABLET, FILM COATED in 1 BOTTLE (50090-4697-2)Nov 7, 2019

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