NDC 70518-4687 – Finasteride

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

Human Prescription Drug

Product NDC70518-4687

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203687
Marketed since
June 30, 2026
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4687-030 POUCH in 1 BOX (70518-4687-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4687-1)Jun 30, 2026

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