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NDC 59651-0484-99

PREDNISONE 1 mg/1 TABLET

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NDC
59651-0484-99
Generic Name
PREDNISONE
Brand Name
PREDNISONE
Strength
1 mg/1
Dosage Form
TABLET
Route
ORAL
Package Size
—
Labeler
Aurobindo Pharma Limited

FDA Drug Information

Indications & Usage

INDICATIONS 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, nonsuppurative thyroiditis, hypercalcemia associated with cancer. Rheumatic disorders : as adjunctive therapy for short-term administration (to tide the patient over an acu…

Important Warnings

WARNINGS: In patients on corticosteroid therapy subject to any 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, suppress the immune system and increase the risk of infection with any pathogen, including viral, bacterial, fungal, p…

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

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Other PREDNISONE NDC Codes

59746-0171-061 mg/1TABLET
2-Day
59746-0171-101 mg/1TABLET
2-Day
59651-0484-011 mg/1TABLET
2-Day
59746-0173-0610 mg/1TABLET
2-Day
59746-0173-1010 mg/1TABLET
2-Day

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