NDC 70518-2287 – Finasteride

Finasteride 1 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC70518-2287

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA207750
Marketed since
August 27, 2019
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (4)

Package NDCDescriptionSince
70518-2287-090 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2287-0)Aug 27, 2019
70518-2287-312 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2287-3)Apr 2, 2026
70518-2287-430 POUCH in 1 BOX (70518-2287-4) / 1 TABLET, COATED in 1 POUCH (70518-2287-5)Jun 9, 2026
70518-2287-650 POUCH in 1 BOX (70518-2287-6) / 1 TABLET, COATED in 1 POUCH (70518-2287-5)Jul 9, 2026

Other Finasteride products