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Hydrocortisone - 0179-0058-70 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 0179-0058
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 10    mg/1 & nbsp;   Hydrocortisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 0179-0058
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040761
Marketing Category: ANDA
Start Marketing Date: 20100305

Package Information of Hydrocortisone

Package NDC: 0179-0058-70
Package Description: 30 TABLET in 1 BOX, UNIT-DOSE (0179-0058-70)

NDC Information of Hydrocortisone

NDC Code 0179-0058-70
Proprietary Name Hydrocortisone
Package Description 30 TABLET in 1 BOX, UNIT-DOSE (0179-0058-70)
Product NDC 0179-0058
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100305
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name HYDROCORTISONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


General Information