NDC 70518-3600 – Finasteride

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

Human Prescription Drug

Product NDC70518-3600

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204304
Marketed since
December 28, 2022
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (3)

Package NDCDescriptionSince
70518-3600-130 POUCH in 1 BOX (70518-3600-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3600-0)Dec 28, 2022
70518-3600-330 TABLET, FILM COATED in 1 BLISTER PACK (70518-3600-3)May 1, 2023
70518-3600-450 POUCH in 1 BOX (70518-3600-4) / 1 TABLET, FILM COATED in 1 POUCH (70518-3600-0)Jul 8, 2026

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