51655-0972 Prednisone

Product NDC:

51655-0972

Brand Name:

Prednisone

Generic Name:

PREDNISONE

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 10.0

Unit: mg/1

Packages:

Code: 51655-0972-20

Description: 20 TABLET in 1 BOTTLE, PLASTIC (51655-972-20)

Effective Date: Sept. 22, 2022

Discontinued:

Code: 51655-0972-21

Description: 21 TABLET in 1 BOTTLE, PLASTIC (51655-972-21)

Effective Date: Dec. 21, 2022

Discontinued:

Code: 51655-0972-27

Description: 12 TABLET in 1 BOTTLE, PLASTIC (51655-972-27)

Effective Date: Feb. 28, 2023

Discontinued:

Code: 51655-0972-51

Description: 40 TABLET in 1 BOTTLE, PLASTIC (51655-972-51)

Effective Date: Oct. 7, 2022

Discontinued:

Code: 51655-0972-52

Description: 30 TABLET in 1 BOTTLE, PLASTIC (51655-972-52)

Effective Date: Sept. 23, 2022

Discontinued:

Code: 51655-0972-53

Description: 10 TABLET in 1 BOTTLE, PLASTIC (51655-972-53)

Effective Date: Dec. 21, 2022

Discontinued:

Code: 51655-0972-54

Description: 15 TABLET in 1 BOTTLE, PLASTIC (51655-972-54)

Effective Date: Dec. 21, 2022

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