51079-0520 Finasteride

Product NDC:

51079-0520

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: 51079-0520-01

Description:

Effective Date: Oct. 22, 2007

Discontinued: Aug. 31, 2015

Code: 51079-0520-20

Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-520-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-520-01)

Effective Date: Oct. 22, 2007

Discontinued: Aug. 31, 2015

Code: 51079-0520-30

Description:

Effective Date: Oct. 22, 2007

Discontinued: Aug. 31, 2015

Code: 51079-0520-56

Description: 10 DOSE PACK in 1 BOX, UNIT-DOSE (51079-520-56) > 30 BLISTER PACK in 1 DOSE PACK (51079-520-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-520-01)

Effective Date: Oct. 26, 2009

Discontinued: July 31, 2015

SEER*Rx Category:

Ancillary Therapy

Major Class:

Protective Agent

Minor Class:

5-alpha Reductase Inhibitor

Orphan Drug Designation:

Status:

No Longer Used

Government Funding Lapse

CanMED: NDC

CanMED and the Oncology Toolbox

CanMED: NDC