54569-0331 Prednisone

Product NDC:

54569-0331

Brand Name:

Prednisone

Generic Name:

Prednisone

Dosage Form Name:

Tablet

Administration Route:

Oral

Substances:

Name: Prednisone

Strength: 10.0

Unit: mg/1

Packages:

Code: 54569-0331-00

Description: 10 TABLET in 1 BOTTLE, GLASS (54569-0331-0)

Effective Date: Feb. 13, 2003

Discontinued:

Code: 54569-0331-01

Description: 15 TABLET in 1 BOTTLE, GLASS (54569-0331-1)

Effective Date: Feb. 13, 2003

Discontinued:

Code: 54569-0331-02

Description: 21 TABLET in 1 BOTTLE, GLASS (54569-0331-2)

Effective Date: Feb. 13, 2003

Discontinued:

Code: 54569-0331-04

Description: 50 TABLET in 1 BOTTLE, GLASS (54569-0331-4)

Effective Date: Feb. 13, 2003

Discontinued:

Code: 54569-0331-05

Description: 30 TABLET in 1 BOTTLE, GLASS (54569-0331-5)

Effective Date: Feb. 13, 2003

Discontinued:

Code: 54569-0331-07

Description: 100 TABLET in 1 BOTTLE, GLASS (54569-0331-7)

Effective Date: Feb. 13, 2003

Discontinued:

Code: 54569-0331-08

Description: 40 TABLET in 1 BOTTLE, GLASS (54569-0331-8)

Effective Date: Feb. 13, 2003

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