70934-0096 Prednisone

Product NDC:

70934-0096

Brand Name:

Prednisone

Generic Name:

Prednisone

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 20.0

Unit: mg/1

Packages:

Code: 70934-0096-06

Description: 6 TABLET in 1 BOTTLE, PLASTIC (70934-096-06)

Effective Date: June 2, 2022

Discontinued:

Code: 70934-0096-10

Description: 10 TABLET in 1 BOTTLE, PLASTIC (70934-096-10)

Effective Date: April 5, 2018

Discontinued:

Code: 70934-0096-12

Description: 12 TABLET in 1 BOTTLE, PLASTIC (70934-096-12)

Effective Date: Sept. 29, 2021

Discontinued:

Code: 70934-0096-15

Description: 15 TABLET in 1 BOTTLE, PLASTIC (70934-096-15)

Effective Date: July 18, 2018

Discontinued:

Code: 70934-0096-20

Description: 20 TABLET in 1 BOTTLE, PLASTIC (70934-096-20)

Effective Date: April 5, 2018

Discontinued:

Code: 70934-0096-21

Description: 21 TABLET in 1 BOTTLE, PLASTIC (70934-096-21)

Effective Date: Aug. 24, 2021

Discontinued:

Code: 70934-0096-30

Description: 30 TABLET in 1 BOTTLE, PLASTIC (70934-096-30)

Effective Date: April 16, 2018

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