68382-0074 Finasteride

Product NDC:

68382-0074

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: 68382-0074-01

Description: 100 TABLET, FILM COATED in 1 BOTTLE (68382-074-01)

Effective Date: Dec. 5, 2017

Discontinued:

Code: 68382-0074-06

Description: 30 TABLET, FILM COATED in 1 BOTTLE (68382-074-06)

Effective Date: Dec. 5, 2017

Discontinued:

Code: 68382-0074-10

Description: 1000 TABLET, FILM COATED in 1 BOTTLE (68382-074-10)

Effective Date: Dec. 5, 2017

Discontinued:

Code: 68382-0074-30

Description: 10 BLISTER PACK in 1 CARTON (68382-074-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: Dec. 5, 2017

Discontinued: Dec. 3, 2019

Code: 68382-0074-77

Description: 10 BLISTER PACK in 1 CARTON (68382-074-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: Dec. 5, 2017

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