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Hydrocortisone - 68788-9922-2 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 68788-9922
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: 68788-9922
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085025
Marketing Category: ANDA
Start Marketing Date: 20120127

Package Information of Hydrocortisone

Package NDC: 68788-9922-2
Package Description: 1 TUBE in 1 CARTON (68788-9922-2) > 28 g in 1 TUBE

NDC Information of Hydrocortisone

NDC Code 68788-9922-2
Proprietary Name Hydrocortisone
Package Description 1 TUBE in 1 CARTON (68788-9922-2) > 28 g in 1 TUBE
Product NDC 68788-9922
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120127
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
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