NDC 65862-149 – Finasteride

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

Human Prescription Drug

Product NDC65862-149

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078341
Marketed since
October 30, 2007
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (4)

Package NDCDescriptionSince
65862-149-01100 TABLET, FILM COATED in 1 BOTTLE (65862-149-01)Oct 30, 2007
65862-149-05500 TABLET, FILM COATED in 1 BOTTLE (65862-149-05)Oct 30, 2007
65862-149-3030 TABLET, FILM COATED in 1 BOTTLE (65862-149-30)Oct 30, 2007
65862-149-9090 TABLET, FILM COATED in 1 BOTTLE (65862-149-90)Oct 30, 2007

Other Finasteride products