NDC 67877-288 – Finasteride

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

Human Prescription Drug

Product NDC67877-288

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204304
Marketed since
January 5, 2017
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (6)

Package NDCDescriptionSince
67877-288-01100 TABLET, FILM COATED in 1 BOTTLE (67877-288-01)Jan 5, 2017
67877-288-05500 TABLET, FILM COATED in 1 BOTTLE (67877-288-05)Jan 5, 2017
67877-288-101000 TABLET, FILM COATED in 1 BOTTLE (67877-288-10)Jan 5, 2017
67877-288-3030 TABLET, FILM COATED in 1 BOTTLE (67877-288-30)Jan 5, 2017
67877-288-331 BLISTER PACK in 1 CARTON (67877-288-33) / 10 TABLET, FILM COATED in 1 BLISTER PACKNov 30, 2020
67877-288-9090 TABLET, FILM COATED in 1 BOTTLE (67877-288-90)Jan 5, 2017

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