NDC 55111-171 – Finasteride

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

Human Prescription Drug

Product NDC55111-171

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076436
Marketed since
January 2, 2013
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
55111-171-05500 TABLET, FILM COATED in 1 BOTTLE (55111-171-05)Jan 2, 2013
55111-171-18180 TABLET, FILM COATED in 1 BOTTLE (55111-171-18)Jan 2, 2013
55111-171-3030 TABLET, FILM COATED in 1 BOTTLE (55111-171-30)Jan 2, 2013
55111-171-9090 TABLET, FILM COATED in 1 BOTTLE (55111-171-90)Jan 2, 2013

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