NDC 70518-3616 – Finasteride

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

Human Prescription Drug

Product NDC70518-3616

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078341
Marketed since
January 18, 2023
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
70518-3616-130 POUCH in 1 BOX (70518-3616-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3616-2)Feb 10, 2023
70518-3616-330 TABLET, FILM COATED in 1 BLISTER PACK (70518-3616-3)May 10, 2023
70518-3616-490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-4)Jan 25, 2024
70518-3616-5100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-5)Aug 7, 2024

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