NDC 70518-1704 – Finasteride

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

Human Prescription Drug

Product NDC70518-1704

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078341
Marketed since
November 30, 2018
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (2)

Package NDCDescriptionSince
70518-1704-2100 POUCH in 1 BOX (70518-1704-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-1704-3)May 26, 2026
70518-1704-450 POUCH in 1 BOX (70518-1704-4) / 1 TABLET, FILM COATED in 1 POUCH (70518-1704-3)Jul 9, 2026

Other Finasteride products