71335-2737 PredniSONE Tablets, USP, 20 mg - CanMED: NDC

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Product Information

CanMED: NDC

Product NDC:

71335-2737

Brand Name:

PredniSONE Tablets, USP, 20 mg

Generic Name:

PredniSONE

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 20.0

Unit: mg/1

Packages:

Code: 71335-2737-00

Description: 100 TABLET in 1 BOTTLE (71335-2737-0)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-01

Description: 6 TABLET in 1 BOTTLE (71335-2737-1)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-02

Description: 14 TABLET in 1 BOTTLE (71335-2737-2)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-03

Description: 5 TABLET in 1 BOTTLE (71335-2737-3)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-04

Description: 10 TABLET in 1 BOTTLE (71335-2737-4)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-05

Description: 8 TABLET in 1 BOTTLE (71335-2737-5)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-06

Description: 7 TABLET in 1 BOTTLE (71335-2737-6)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-07

Description: 24 TABLET in 1 BOTTLE (71335-2737-7)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-08

Description: 90 TABLET in 1 BOTTLE (71335-2737-8)

Effective Date: Sept. 26, 2025

Discontinued:

Code: 71335-2737-09

Description: 12 TABLET in 1 BOTTLE (71335-2737-9)

Effective Date: Sept. 26, 2025

Discontinued:

SEER*Rx Category:

Hormonal Therapy

Major Class:

Adrenal Glucocorticoid

Minor Class:

Corticosteroid

Orphan Drug Designation:

Status:

In Use