55111-0172 Finasteride

Product NDC:

55111-0172

Brand Name:

Finasteride

Generic Name:

Finasteride

Dosage Form Name:

Tablet

Administration Route:

Oral

Substances:

Name: Finasteride

Strength: 5.0

Unit: mg/1

Packages:

Code: 55111-0172-01

Description: 100 TABLET in 1 BOTTLE (55111-172-01)

Effective Date: Feb. 28, 2007

Discontinued:

Code: 55111-0172-05

Description: 500 TABLET in 1 BOTTLE (55111-172-05)

Effective Date: Feb. 28, 2007

Discontinued:

Code: 55111-0172-30

Description: 30 TABLET in 1 BOTTLE (55111-172-30)

Effective Date: Feb. 28, 2007

Discontinued:

Code: 55111-0172-78

Description: 10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79)

Effective Date: Feb. 28, 2007

Discontinued:

Code: 55111-0172-79

Description:

Effective Date: Feb. 28, 2007

Discontinued:

Code: 55111-0172-90

Description: 90 TABLET in 1 BOTTLE (55111-172-90)

Effective Date: Feb. 28, 2007

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

CanMED: NDC