71335-2754 PredniSONE Tablets, USP, 20 mg - CanMED: NDC

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Product Information

CanMED: NDC

Product NDC:

71335-2754

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: 71335-2754-00

Description: 11 TABLET in 1 BOTTLE (71335-2754-0)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-01

Description: 20 TABLET in 1 BOTTLE (71335-2754-1)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-02

Description: 30 TABLET in 1 BOTTLE (71335-2754-2)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-03

Description: 40 TABLET in 1 BOTTLE (71335-2754-3)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-04

Description: 15 TABLET in 1 BOTTLE (71335-2754-4)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-05

Description: 10 TABLET in 1 BOTTLE (71335-2754-5)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-06

Description: 21 TABLET in 1 BOTTLE (71335-2754-6)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-07

Description: 18 TABLET in 1 BOTTLE (71335-2754-7)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-08

Description: 12 TABLET in 1 BOTTLE (71335-2754-8)

Effective Date: Oct. 3, 2025

Discontinued:

Code: 71335-2754-09

Description: 23 TABLET in 1 BOTTLE (71335-2754-9)

Effective Date: Oct. 3, 2025

Discontinued:

SEER*Rx Category:

Hormonal Therapy

Major Class:

Adrenal Glucocorticoid

Minor Class:

Corticosteroid

Orphan Drug Designation:

Status:

In Use