47335-0715 Finasteride

Product NDC:

47335-0715

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: 47335-0715-08

Description: 100 TABLET, FILM COATED in 1 BOTTLE (47335-715-08)

Effective Date: Nov. 25, 2022

Discontinued:

Code: 47335-0715-13

Description: 500 TABLET, FILM COATED in 1 BOTTLE (47335-715-13)

Effective Date: Nov. 25, 2022

Discontinued:

Code: 47335-0715-18

Description: 1000 TABLET, FILM COATED in 1 BOTTLE (47335-715-18)

Effective Date: Nov. 25, 2022

Discontinued:

Code: 47335-0715-81

Description: 90 TABLET, FILM COATED in 1 BOTTLE (47335-715-81)

Effective Date: Nov. 25, 2022

Discontinued:

Code: 47335-0715-83

Description: 30 TABLET, FILM COATED in 1 BOTTLE (47335-715-83)

Effective Date: Nov. 25, 2022

Discontinued:

Code: 47335-0715-88

Description: 100 TABLET, FILM COATED in 1 BOTTLE (47335-715-88)

Effective Date: Nov. 25, 2022

Discontinued:

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