NDC 0615-8562 – Finasteride

Finasteride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0615-8562

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076437
Marketed since
February 28, 2007
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
0615-8562-0515 TABLET in 1 BLISTER PACK (0615-8562-05)Feb 11, 2025
0615-8562-3930 TABLET in 1 BLISTER PACK (0615-8562-39)Feb 11, 2025

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