70518-0242 Prednisone

Product NDC:

70518-0242

Brand Name:

Prednisone

Generic Name:

Prednisone

Dosage Form Name:

Tablet

Administration Route:

Oral

Substances:

Name: Prednisone

Strength: 20.0

Unit: mg/1

Packages:

Code: 70518-0242-00

Description: 16 TABLET in 1 BOTTLE, PLASTIC (70518-0242-0)

Effective Date: Feb. 20, 2017

Discontinued:

Code: 70518-0242-01

Description: 10 TABLET in 1 BOTTLE, PLASTIC (70518-0242-1)

Effective Date: Feb. 20, 2017

Discontinued:

Code: 70518-0242-02

Description: 30 TABLET in 1 BOTTLE, PLASTIC (70518-0242-2)

Effective Date: July 21, 2017

Discontinued:

Code: 70518-0242-03

Description: 15 TABLET in 1 BOTTLE, PLASTIC (70518-0242-3)

Effective Date: July 25, 2018

Discontinued:

Code: 70518-0242-04

Description: 48 TABLET in 1 BOTTLE, PLASTIC (70518-0242-4)

Effective Date: Oct. 3, 2018

Discontinued:

Code: 70518-0242-05

Description: 14 TABLET in 1 BOTTLE, PLASTIC (70518-0242-5)

Effective Date: April 1, 2019

Discontinued:

SEER*Rx Category:

Hormonal Therapy

Major Class:

Adrenal Glucocorticoid

Minor Class:

Corticosteroid

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox

CanMED: NDC