NDC 50090-7228 – Finasteride

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

Human Prescription Drug

Product NDC50090-7228

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090061
Marketed since
June 13, 2015
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
50090-7228-012 BOTTLE in 1 CASE (50090-7228-0) / 30 TABLET, FILM COATED in 1 BOTTLEAug 22, 2024

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