67877-0288 Finasteride

Product NDC:

67877-0288

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: 67877-0288-01

Description: 100 TABLET, FILM COATED in 1 BOTTLE (67877-288-01)

Effective Date: Jan. 5, 2017

Discontinued:

Code: 67877-0288-05

Description: 500 TABLET, FILM COATED in 1 BOTTLE (67877-288-05)

Effective Date: Jan. 5, 2017

Discontinued:

Code: 67877-0288-10

Description: 1000 TABLET, FILM COATED in 1 BOTTLE (67877-288-10)

Effective Date: Jan. 5, 2017

Discontinued:

Code: 67877-0288-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (67877-288-30)

Effective Date: Jan. 5, 2017

Discontinued:

Code: 67877-0288-33

Description: 1 BLISTER PACK in 1 CARTON (67877-288-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: Nov. 30, 2020

Discontinued:

Code: 67877-0288-90

Description: 90 TABLET, FILM COATED in 1 BOTTLE (67877-288-90)

Effective Date: Jan. 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

CanMED: NDC