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Hydrocortisone - 54868-1743-3 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 54868-1743
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 20    mg/1 & nbsp;   Hydrocortisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 54868-1743
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083365
Marketing Category: ANDA
Start Marketing Date: 20070705

Package Information of Hydrocortisone

Package NDC: 54868-1743-3
Package Description: 30 TABLET in 1 BOTTLE (54868-1743-3)

NDC Information of Hydrocortisone

NDC Code 54868-1743-3
Proprietary Name Hydrocortisone
Package Description 30 TABLET in 1 BOTTLE (54868-1743-3)
Product NDC 54868-1743
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070705
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDROCORTISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


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