NDC 55111-172 – Finasteride

Finasteride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC55111-172

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076437
Marketed since
February 28, 2007
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (5)

Package NDCDescriptionSince
55111-172-01100 TABLET in 1 BOTTLE (55111-172-01)Feb 28, 2007
55111-172-05500 TABLET in 1 BOTTLE (55111-172-05)Feb 28, 2007
55111-172-3030 TABLET in 1 BOTTLE (55111-172-30)Feb 28, 2007
55111-172-7810 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79)Feb 28, 2007
55111-172-9090 TABLET in 1 BOTTLE (55111-172-90)Feb 28, 2007

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