NDC 70518-3182 – Finasteride

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

Human Prescription Drug

Product NDC70518-3182

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090061
Marketed since
August 5, 2021
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
70518-3182-030 POUCH in 1 BOX (70518-3182-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3182-1)Aug 5, 2021

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