65862-0149 Finasteride

Product NDC:

65862-0149

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: 65862-0149-01

Description: 100 TABLET, FILM COATED in 1 BOTTLE (65862-149-01)

Effective Date: Oct. 30, 2007

Discontinued:

Code: 65862-0149-05

Description: 500 TABLET, FILM COATED in 1 BOTTLE (65862-149-05)

Effective Date: Oct. 30, 2007

Discontinued:

Code: 65862-0149-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (65862-149-30)

Effective Date: Oct. 30, 2007

Discontinued:

Code: 65862-0149-61

Description:

Effective Date: June 30, 2011

Discontinued: Oct. 25, 2011

Code: 65862-0149-90

Description: 90 TABLET, FILM COATED in 1 BOTTLE (65862-149-90)

Effective Date: Oct. 30, 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