NDC 76282-412 – Finasteride

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

Human Prescription Drug

Product NDC76282-412

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Exelan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090061
Marketed since
May 22, 2015
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (4)

Package NDCDescriptionSince
76282-412-05500 TABLET, FILM COATED in 1 BOTTLE (76282-412-05)May 22, 2015
76282-412-101000 TABLET, FILM COATED in 1 BOTTLE (76282-412-10)May 22, 2015
76282-412-3030 TABLET, FILM COATED in 1 BOTTLE (76282-412-30)May 22, 2015
76282-412-9090 TABLET, FILM COATED in 1 BOTTLE (76282-412-90)May 22, 2015

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