NDC 71610-515 – Finasteride

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

Human Prescription Drug

Product NDC71610-515

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090061
Marketed since
May 22, 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 (3)

Package NDCDescriptionSince
71610-515-3030 TABLET, FILM COATED in 1 BOTTLE (71610-515-30)Apr 3, 2024
71610-515-5360 TABLET, FILM COATED in 1 BOTTLE (71610-515-53)Apr 3, 2024
71610-515-6090 TABLET, FILM COATED in 1 BOTTLE (71610-515-60)Jan 8, 2021

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