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Hydrocortisone - 54569-1154-0 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 54569-1154
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 25    mg/g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 54569-1154
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089414
Marketing Category: ANDA
Start Marketing Date: 19861216

Package Information of Hydrocortisone

Package NDC: 54569-1154-0
Package Description: 30 g in 1 TUBE (54569-1154-0)

NDC Information of Hydrocortisone

NDC Code 54569-1154-0
Proprietary Name Hydrocortisone
Package Description 30 g in 1 TUBE (54569-1154-0)
Product NDC 54569-1154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19861216
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name HYDROCORTISONE
Strength Number 25
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


General Information