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NDC 64380-0949-06

PREDNISONE 50 mg/1 TABLET

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NDC
64380-0949-06
Generic Name
PREDNISONE
Brand Name
prednisone
Strength
50 mg/1
Dosage Form
TABLET
Route
ORAL
Package Size
—
Labeler
Strides Pharma Science Limited

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Prednisone tablets USP are indicated in the following conditions: Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice: synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance); congenital adrenal hyperplasia; hypercalcemia associated with cancer; nonsuppurative thyroiditis. Rheumatic Disorders As adjunctiv…

Important Warnings

WARNINGS In patients on corticosteroid therapy subjected to unusual stress, increased dosage of rapidly acting corticosteroids before, during and after the stressful situation is indicated. Immunosuppression and Increased Risk of Infection Corticosteroids, including prednisone tablets, suppress the immune system and increase the risk of infection with any pathogen, including viral, bacterial, fung…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other PREDNISONE NDC Codes

59746-0171-101 mg/1TABLET
2-Day
59651-0484-011 mg/1TABLET
2-Day
59651-0484-991 mg/1TABLET
2-Day
59746-0171-061 mg/1TABLET
2-Day
59746-0173-0610 mg/1TABLET
2-Day

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