51079-0321 Finasteride

Product NDC:

51079-0321

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: 51079-0321-01

Description:

Effective Date: July 13, 2015

Discontinued: June 30, 2019

Code: 51079-0321-20

Description: 100 BLISTER PACK in 1 CARTON (51079-321-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-321-01)

Effective Date: July 13, 2015

Discontinued: June 30, 2019

Code: 51079-0321-30

Description:

Effective Date: July 13, 2015

Discontinued: June 30, 2019

Code: 51079-0321-56

Description: 10 DOSE PACK in 1 CARTON (51079-321-56) > 30 BLISTER PACK in 1 DOSE PACK (51079-321-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-321-01)

Effective Date: July 17, 2015

Discontinued: Dec. 31, 2018

SEER*Rx Category:

Ancillary Therapy

Major Class:

Protective Agent

Minor Class:

5-alpha Reductase Inhibitor

Orphan Drug Designation:

Status:

No Longer Used

CanMED and the Oncology Toolbox

CanMED: NDC