68788-4182 PredniSONE

Product NDC:

68788-4182

Brand Name:

PredniSONE

Generic Name:

PredniSONE

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 20.0

Unit: mg/1

Packages:

Code: 68788-4182-01

Description: 10 TABLET in 1 BOTTLE, PLASTIC (68788-4182-1)

Effective Date: Aug. 20, 2026

Discontinued:

Code: 68788-4182-02

Description: 20 TABLET in 1 BOTTLE, PLASTIC (68788-4182-2)

Effective Date: Aug. 20, 2026

Discontinued:

Code: 68788-4182-03

Description: 30 TABLET in 1 BOTTLE, PLASTIC (68788-4182-3)

Effective Date: Aug. 20, 2026

Discontinued:

Code: 68788-4182-04

Description: 18 TABLET in 1 BOTTLE, PLASTIC (68788-4182-4)

Effective Date: Aug. 20, 2026

Discontinued:

Code: 68788-4182-05

Description: 15 TABLET in 1 BOTTLE, PLASTIC (68788-4182-5)

Effective Date: Aug. 20, 2026

Discontinued:

Code: 68788-4182-08

Description: 21 TABLET in 1 BOTTLE, PLASTIC (68788-4182-8)

Effective Date: Aug. 20, 2026

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