NDC 55154-8083 – Finasteride

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

Human Prescription Drug

Product NDC55154-8083

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Cardinal Health 107, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090061
Marketed since
June 13, 2015
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
55154-8083-010 BLISTER PACK in 1 BAG (55154-8083-0) / 1 TABLET, FILM COATED in 1 BLISTER PACKJun 13, 2015

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