71335-2079 Prednisone

Product NDC:

71335-2079

Brand Name:

Prednisone

Generic Name:

PREDNISONE

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: PREDNISONE

Strength: 20.0

Unit: mg/1

Packages:

Code: 71335-2079-00

Description: 11 TABLET in 1 BOTTLE, PLASTIC (71335-2079-0)

Effective Date: May 3, 2022

Discontinued:

Code: 71335-2079-01

Description: 20 TABLET in 1 BOTTLE, PLASTIC (71335-2079-1)

Effective Date: May 6, 2022

Discontinued:

Code: 71335-2079-02

Description: 30 TABLET in 1 BOTTLE, PLASTIC (71335-2079-2)

Effective Date: May 31, 2022

Discontinued:

Code: 71335-2079-03

Description: 40 TABLET in 1 BOTTLE, PLASTIC (71335-2079-3)

Effective Date: Sept. 6, 2022

Discontinued:

Code: 71335-2079-04

Description: 15 TABLET in 1 BOTTLE, PLASTIC (71335-2079-4)

Effective Date: June 9, 2022

Discontinued:

Code: 71335-2079-05

Description: 10 TABLET in 1 BOTTLE, PLASTIC (71335-2079-5)

Effective Date: April 27, 2022

Discontinued:

Code: 71335-2079-06

Description: 21 TABLET in 1 BOTTLE, PLASTIC (71335-2079-6)

Effective Date: June 2, 2022

Discontinued:

Code: 71335-2079-07

Description: 18 TABLET in 1 BOTTLE, PLASTIC (71335-2079-7)

Effective Date: June 23, 2022

Discontinued:

Code: 71335-2079-08

Description: 12 TABLET in 1 BOTTLE, PLASTIC (71335-2079-8)

Effective Date: April 18, 2022

Discontinued:

Code: 71335-2079-09

Description: 23 TABLET in 1 BOTTLE, PLASTIC (71335-2079-9)

Effective Date: April 3, 2024

Discontinued:

SEER*Rx Category:

Hormonal Therapy

Major Class:

Adrenal Glucocorticoid

Minor Class:

Corticosteroid

Orphan Drug Designation:

Status:

In Use

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