31722-0525 Finasteride

Product NDC:

31722-0525

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: 31722-0525-01

Description: 100 TABLET, FILM COATED in 1 BOTTLE (31722-525-01)

Effective Date: Aug. 1, 2010

Discontinued:

Code: 31722-0525-05

Description: 500 TABLET, FILM COATED in 1 BOTTLE (31722-525-05)

Effective Date: Aug. 1, 2010

Discontinued:

Code: 31722-0525-10

Description: 1000 TABLET, FILM COATED in 1 BOTTLE (31722-525-10)

Effective Date: Aug. 1, 2010

Discontinued:

Code: 31722-0525-30

Description: 12 BOTTLE in 1 CASE (31722-525-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Effective Date: Aug. 1, 2010

Discontinued:

Code: 31722-0525-90

Description: 12 BOTTLE in 1 CASE (31722-525-90) / 90 TABLET, FILM COATED in 1 BOTTLE

Effective Date: Aug. 1, 2010

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Protective Agent

Minor Class:

5-alpha Reductase Inhibitor

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox