NDC 0093-7355 – Finasteride

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

Human Prescription Drug

Product NDC0093-7355

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076511
Marketed since
December 15, 2006
Marketing end
September 30, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (3)

Package NDCDescriptionSince
0093-7355-05500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05)Mar 14, 2008
0093-7355-5630 TABLET, FILM COATED in 1 BOTTLE (0093-7355-56)Dec 15, 2006
0093-7355-9890 TABLET, FILM COATED in 1 BOTTLE (0093-7355-98)Feb 22, 2007

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