50742-0123 Finasteride

Product NDC:

50742-0123

Brand Name:

Finasteride

Generic Name:

Finasteride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: Finasteride

Strength: 5.0

Unit: mg/1

Packages:

Code: 50742-0123-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (50742-123-30)

Effective Date: Aug. 1, 2011

Discontinued: Jan. 31, 2015

Code: 50742-0123-90

Description: 90 TABLET, FILM COATED in 1 BOTTLE (50742-123-90)

Effective Date: Aug. 1, 2011

Discontinued: Jan. 31, 2015

SEER*Rx Category:

Ancillary Therapy

Major Class:

Protective Agent

Minor Class:

5-alpha Reductase Inhibitor

Orphan Drug Designation:

Status:

No Longer Used

CanMED and the Oncology Toolbox