00093-7355 Finasteride

Product NDC:

00093-7355

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: 00093-7355-01

Description:

Effective Date: Dec. 15, 2006

Discontinued: Aug. 5, 2013

Code: 00093-7355-05

Description: 500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05)

Effective Date: March 14, 2008

Discontinued:

Code: 00093-7355-56

Description: 30 TABLET, FILM COATED in 1 BOTTLE (0093-7355-56)

Effective Date: Dec. 15, 2006

Discontinued:

Code: 00093-7355-98

Description: 90 TABLET, FILM COATED in 1 BOTTLE (0093-7355-98)

Effective Date: Feb. 22, 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