NDC 71335-1304 – Finasteride

Finasteride 1 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-1304

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA207750
Marketed since
January 6, 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 (5)

Package NDCDescriptionSince
71335-1304-130 TABLET, COATED in 1 BOTTLE (71335-1304-1)Aug 16, 2019
71335-1304-290 TABLET, COATED in 1 BOTTLE (71335-1304-2)Aug 16, 2019
71335-1304-360 TABLET, COATED in 1 BOTTLE (71335-1304-3)Nov 20, 2019
71335-1304-428 TABLET, COATED in 1 BOTTLE (71335-1304-4)May 30, 2024
71335-1304-5180 TABLET, COATED in 1 BOTTLE (71335-1304-5)Jun 5, 2020

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