50268-0323 Finasteride

Product NDC:

50268-0323

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: 50268-0323-11

Description:

Effective Date: March 21, 2011

Discontinued: July 31, 2019

Code: 50268-0323-15

Description: 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-323-15) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-323-11)

Effective Date: March 21, 2011

Discontinued: July 31, 2019

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