70934-0291 Prednisone

Product NDC:

70934-0291

Brand Name:

Prednisone

Generic Name:

Prednisone

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 10.0

Unit: mg/1

Packages:

Code: 70934-0291-12

Description: 12 TABLET in 1 BOTTLE, PLASTIC (70934-291-12)

Effective Date: Jan. 9, 2020

Discontinued:

Code: 70934-0291-15

Description: 15 TABLET in 1 BOTTLE, PLASTIC (70934-291-15)

Effective Date: Jan. 9, 2020

Discontinued:

Code: 70934-0291-20

Description: 20 TABLET in 1 BOTTLE, PLASTIC (70934-291-20)

Effective Date: March 21, 2019

Discontinued:

Code: 70934-0291-21

Description: 21 TABLET in 1 BOTTLE, PLASTIC (70934-291-21)

Effective Date: Sept. 6, 2019

Discontinued:

Code: 70934-0291-30

Description: 30 TABLET in 1 BOTTLE, PLASTIC (70934-291-30)

Effective Date: Feb. 21, 2019

Discontinued: Jan. 31, 2024

Code: 70934-0291-40

Description: 40 TABLET in 1 BOTTLE, PLASTIC (70934-291-40)

Effective Date: Jan. 9, 2020

Discontinued:

Code: 70934-0291-42

Description: 42 TABLET in 1 BOTTLE, PLASTIC (70934-291-42)

Effective Date: Jan. 9, 2020

Discontinued:

SEER*Rx Category:

Hormonal Therapy

Major Class:

Adrenal Glucocorticoid

Minor Class:

Corticosteroid

Orphan Drug Designation:

Status:

No Longer Used

CanMED and the Oncology Toolbox

CanMED: NDC