NDC 67877-455 – Finasteride

Finasteride 1 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC67877-455

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA207750
Marketed since
January 6, 2017
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
67877-455-05500 TABLET, COATED in 1 BOTTLE (67877-455-05)Jan 31, 2025
67877-455-3030 TABLET, COATED in 1 BOTTLE (67877-455-30)Jan 6, 2017
67877-455-9090 TABLET, COATED in 1 BOTTLE (67877-455-90)Jan 6, 2017
67877-455-943 BLISTER PACK in 1 CARTON (67877-455-94) / 10 TABLET, COATED in 1 BLISTER PACK (67877-455-34)Jan 6, 2017

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