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Hydrocortisone - 0168-0080-31 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 0168-0080
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: 0168-0080
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089414
Marketing Category: ANDA
Start Marketing Date: 19861216

Package Information of Hydrocortisone

Package NDC: 0168-0080-31
Package Description: 30 g in 1 TUBE (0168-0080-31)

NDC Information of Hydrocortisone

NDC Code 0168-0080-31
Proprietary Name Hydrocortisone
Package Description 30 g in 1 TUBE (0168-0080-31)
Product NDC 0168-0080
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 E. FOUGERA & CO. A division of Fougera 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