72789-0473 PredniSONE Tablets, USP, 20 mg

Product NDC:

72789-0473

Brand Name:

PredniSONE Tablets, USP, 20 mg

Generic Name:

PredniSONE

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 20.0

Unit: mg/1

Packages:

Code: 72789-0473-01

Description: 100 TABLET in 1 BOTTLE, PLASTIC (72789-473-01)

Effective Date: May 22, 2025

Discontinued:

Code: 72789-0473-95

Description: 1000 TABLET in 1 BOTTLE, PLASTIC (72789-473-95)

Effective Date: May 22, 2025

Discontinued:

Code: 72789-0473-25

Description: 25 TABLET in 1 BOTTLE, PLASTIC (72789-473-25)

Effective Date: May 22, 2025

Discontinued:

Code: 72789-0473-21

Description: 21 TABLET in 1 BOTTLE, PLASTIC (72789-473-21)

Effective Date: May 22, 2025

Discontinued:

Code: 72789-0473-30

Description: 30 TABLET in 1 BOTTLE, PLASTIC (72789-473-30)

Effective Date: May 30, 2025

Discontinued:

Code: 72789-0473-05

Description: 5 TABLET in 1 BOTTLE, PLASTIC (72789-473-05)

Effective Date: June 9, 2025

Discontinued:

Code: 72789-0473-10

Description: 10 TABLET in 1 BOTTLE, PLASTIC (72789-473-10)

Effective Date: June 10, 2025

Discontinued:

Code: 72789-0473-20

Description: 20 TABLET in 1 BOTTLE, PLASTIC (72789-473-20)

Effective Date: June 9, 2025

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