70518-3616 Finasteride

Product NDC:

70518-3616

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: 70518-3616-00

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3616-0)

Effective Date: Jan. 18, 2023

Discontinued:

Code: 70518-3616-01

Description: 30 POUCH in 1 BOX (70518-3616-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3616-2)

Effective Date: Feb. 10, 2023

Discontinued:

Code: 70518-3616-03

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3616-3)

Effective Date: May 10, 2023

Discontinued:

Code: 70518-3616-04

Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-4)

Effective Date: Jan. 25, 2024

Discontinued:

Code: 70518-3616-05

Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-5)

Effective Date: Aug. 7, 2024

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Protective Agent

Minor Class:

5-alpha Reductase Inhibitor

Orphan Drug Designation:

No

Status:

In Use

CanMED and the Oncology Toolbox