72789-0401 Prednisone

Product NDC:

72789-0401

Brand Name:

Prednisone

Generic Name:

Prednisone

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 10.0

Unit: mg/1

Packages:

Code: 72789-0401-10

Description: 10 TABLET in 1 BOTTLE, PLASTIC (72789-401-10)

Effective Date: June 4, 2024

Discontinued:

Code: 72789-0401-30

Description: 30 TABLET in 1 BOTTLE, PLASTIC (72789-401-30)

Effective Date: June 3, 2024

Discontinued:

Code: 72789-0401-40

Description: 40 TABLET in 1 BOTTLE, PLASTIC (72789-401-40)

Effective Date: June 3, 2024

Discontinued:

Code: 72789-0401-50

Description: 50 TABLET in 1 BOTTLE, PLASTIC (72789-401-50)

Effective Date: June 3, 2024

Discontinued:

Code: 72789-0401-21

Description: 21 TABLET in 1 BOTTLE, PLASTIC (72789-401-21)

Effective Date: June 25, 2024

Discontinued:

Code: 72789-0401-20

Description: 20 TABLET in 1 BOTTLE, PLASTIC (72789-401-20)

Effective Date: June 20, 2024

Discontinued:

Code: 72789-0401-12

Description: 12 TABLET in 1 BOTTLE, PLASTIC (72789-401-12)

Effective Date: July 10, 2024

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