71335-1915 PREDNISONE

Product NDC:

71335-1915

Brand Name:

PREDNISONE

Generic Name:

Prednisone

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 10.0

Unit: mg/1

Packages:

Code: 71335-1915-00

Description: 10 TABLET in 1 BOTTLE, PLASTIC (71335-1915-0)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-01

Description: 21 TABLET in 1 BOTTLE, PLASTIC (71335-1915-1)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-02

Description: 40 TABLET in 1 BOTTLE, PLASTIC (71335-1915-2)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-03

Description: 30 TABLET in 1 BOTTLE, PLASTIC (71335-1915-3)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-04

Description: 20 TABLET in 1 BOTTLE, PLASTIC (71335-1915-4)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-05

Description: 15 TABLET in 1 BOTTLE, PLASTIC (71335-1915-5)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-06

Description: 50 TABLET in 1 BOTTLE, PLASTIC (71335-1915-6)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-07

Description: 60 TABLET in 1 BOTTLE, PLASTIC (71335-1915-7)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-08

Description: 42 TABLET in 1 BOTTLE, PLASTIC (71335-1915-8)

Effective Date: July 20, 2021

Discontinued:

Code: 71335-1915-09

Description: 48 TABLET in 1 BOTTLE, PLASTIC (71335-1915-9)

Effective Date: July 20, 2021

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